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rs707908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs707908(C;G)
Make rs707908(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270276
GeneHLA-C
is asnp
is mentioned by
dbSNPrs707908
ebirs707908
HLIrs707908
Exacrs707908
Varsomers707908
Maprs707908
PheGenIrs707908
hapmaprs707908
1000 genomesrs707908
hgdprs707908
ensemblrs707908
gopubmedrs707908
geneviewrs707908
scholarrs707908
googlers707908
pharmgkbrs707908
gwascentralrs707908
openSNPrs707908
23andMers707908
23andMe allrs707908
SNP Nexus

SNPshotrs707908
SNPdbers707908
MSV3drs707908
GWAS Ctlgrs707908
GMAF0.3439
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs707908(A,G;A,G)
Alt rs707908(A,G;A,G)
Reference rs707908(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238053G>C
CLNSRC
CLNACC