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rs17413685

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17413685(A;A)
Make rs17413685(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271087
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17413685
ebirs17413685
HLIrs17413685
Exacrs17413685
Varsomers17413685
Maprs17413685
PheGenIrs17413685
hapmaprs17413685
1000 genomesrs17413685
hgdprs17413685
ensemblrs17413685
gopubmedrs17413685
geneviewrs17413685
scholarrs17413685
googlers17413685
pharmgkbrs17413685
gwascentralrs17413685
openSNPrs17413685
23andMers17413685
23andMe allrs17413685
SNP Nexus

SNPshotrs17413685
SNPdbers17413685
MSV3drs17413685
GWAS Ctlgrs17413685
Max Magnitude0
ClinVar
Risk rs17413685(A,T;A,T)
Alt rs17413685(A,T;A,T)
Reference rs17413685(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238864G>A; NC_000006.11:g.31238864G>T
CLNSRC
CLNACC