SNP Report
Basic Info
Name |
rs10513219
dbSNP
Ensembl
|
Location |
Chr3:143534874(Fwd) |
Variant Alleles |
G/A |
Ancestral Allele |
A |
Functional Annotation |
NMD_transcript_variant; intron_variant.
|
Consequence to Transcript |
NMD_transcript_variant(ENST00000474727) intron_variant(ENST00000316549; ENST00000474727; ENST00000474151) |
No. of Studies |
1 (significant: 1; non-significant: 0; trend: 0) |
Source |
Literature-origin
|
SNP related studies (count: 1)
SNP related genes (count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.
Literature-origin SNPs (count: 0)
LD-proxies (count: 12)
rs_ID |
Functional Annotation |
r2[population] |
rs11917152
|
NMD_transcript_variant; intron_variant |
0.817[CEU]; 0.85[CHB]; 0.907[TSI]
|
rs7641634
|
NMD_transcript_variant; intron_variant |
0.871[CEU]; 0.85[CHB]; 0.884[TSI]
|
rs2361200
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.897[CHB]; 0.913[CHD]; 1.0[GIH]; 1.0[JPT]; 0.902[LWK]; 0.887[MEX]; 0.928[MKK]; 1.0[TSI]
|
rs6798159
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.85[CHB]
|
rs6794755
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.897[CHB]; 1.0[JPT]
|
rs6773298
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.897[CHB]; 1.0[JPT]
|
rs6806661
|
NMD_transcript_variant; intron_variant |
0.871[CEU]; 0.839[GIH]; 0.81[TSI]
|
rs2011026
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.897[CHB]; 1.0[JPT]
|
rs11918501
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.942[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs1823221
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.897[CHB]; 0.93[JPT]
|
rs11919227
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.897[CHB]; 1.0[JPT]
|
rs11710427
|
NMD_transcript_variant; intron_variant |
1.0[CEU]; 0.893[CHB]; 0.937[CHD]; 1.0[GIH]; 1.0[JPT]; 0.835[MEX]; 1.0[TSI]
|