SNP Report
Basic Info
Name |
rs362553
dbSNP
Ensembl
|
Location |
Chr20:10299223(Fwd) |
Variant Alleles |
G/A |
Ancestral Allele |
G |
Functional Annotation |
intron_variant; nc_transcript_variant.
|
Consequence to Transcript |
intron_variant(ENST00000421143; ENST00000453544) nc_transcript_variant(ENST00000421143; ENST00000453544) |
No. of Studies |
1 (significant: 1; non-significant: 0; trend: 0) |
Source |
Literature-origin
|
SNP related studies (count: 1)
SNP related genes (count: 2)
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: 11)
rs_ID |
Functional Annotation |
r2[population] |
rs6039851
|
intron_variant; nc_transcript_variant |
0.878[CHB]; 0.842[JPT]
|
rs6039848
|
intron_variant; nc_transcript_variant |
0.878[CHB]; 0.842[JPT]; 0.878[MEX]
|
rs362598
|
downstream_gene_variant; intron_variant; nc_transcript_variant |
1.0[ASW]; 1.0[LWK]; 1.0[MKK]; 1.0[YRI]
|
rs6039847
|
intron_variant; nc_transcript_variant |
0.878[CHB]; 0.842[JPT]; 0.878[MEX]
|
rs6131075
|
intron_variant; nc_transcript_variant |
0.878[CHB]; 0.842[JPT]; 1.0[YRI]
|
rs362551
|
intron_variant; nc_transcript_variant |
1.0[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs12625519
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs6133862
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 0.936[CHB]; 0.842[JPT]; 1.0[YRI]
|
rs6133863
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 0.936[CHB]; 0.842[JPT]; 1.0[YRI]
|
rs6133861
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 0.936[CHB]; 0.92[JPT]; 1.0[YRI]
|
rs362554
|
intron_variant; nc_transcript_variant |
1.0[CEU]
|