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rs17886924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17886924(A;A)
Make rs17886924(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270855
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17886924
dbSNP (classic)rs17886924
ClinGenrs17886924
ebirs17886924
HLIrs17886924
Exacrs17886924
Gnomadrs17886924
Varsomers17886924
LitVarrs17886924
Maprs17886924
PheGenIrs17886924
Biobankrs17886924
1000 genomesrs17886924
hgdprs17886924
ensemblrs17886924
geneviewrs17886924
scholarrs17886924
googlers17886924
pharmgkbrs17886924
gwascentralrs17886924
openSNPrs17886924
23andMers17886924
SNPshotrs17886924
SNPdbers17886924
MSV3drs17886924
GWAS Ctlgrs17886924
GMAF0.2121
Max Magnitude0
ClinVar
Risk rs17886924(A;A)
Alt rs17886924(A;A)
Reference Rs17886924(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238632C>T
CLNSRC
CLNACC