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rs7383157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs7383157(G;G)
Make rs7383157(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271529
GeneHLA-C
is asnp
is mentioned by
dbSNPrs7383157
ebirs7383157
HLIrs7383157
Exacrs7383157
Varsomers7383157
Maprs7383157
PheGenIrs7383157
hapmaprs7383157
1000 genomesrs7383157
hgdprs7383157
ensemblrs7383157
gopubmedrs7383157
geneviewrs7383157
scholarrs7383157
googlers7383157
pharmgkbrs7383157
gwascentralrs7383157
openSNPrs7383157
23andMers7383157
23andMe allrs7383157
SNP Nexus

SNPshotrs7383157
SNPdbers7383157
MSV3drs7383157
GWAS Ctlgrs7383157
GMAF0.1543
Max Magnitude0
? (G;G) (G;T) (T;T) 28
ClinVar
Risk rs7383157(G;G)
Alt rs7383157(G;G)
Reference rs7383157(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239306T; NC_000006.11:g.31239306T>G
CLNSRC
CLNACC