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rs697743

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs697743(C;T)
Make rs697743(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271154
GeneHLA-C
is asnp
is mentioned by
dbSNPrs697743
ebirs697743
HLIrs697743
Exacrs697743
Varsomers697743
Maprs697743
PheGenIrs697743
hapmaprs697743
1000 genomesrs697743
hgdprs697743
ensemblrs697743
gopubmedrs697743
geneviewrs697743
scholarrs697743
googlers697743
pharmgkbrs697743
gwascentralrs697743
openSNPrs697743
23andMers697743
23andMe allrs697743
SNP Nexus

SNPshotrs697743
SNPdbers697743
MSV3drs697743
GWAS Ctlgrs697743
Max Magnitude0
ClinVar
Risk rs697743(A,G,T;A,G,T)
Alt rs697743(A,G,T;A,G,T)
Reference rs697743(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238931G>A; NC_000006.11:g.31238931G>C; NC_000006.11:g.31238931G>T
CLNSRC
CLNACC