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rs17850337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs17850337(A;A)
Make rs17850337(A;G)
Make rs17850337(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271234
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17850337
ebirs17850337
HLIrs17850337
Exacrs17850337
Varsomers17850337
Maprs17850337
PheGenIrs17850337
hapmaprs17850337
1000 genomesrs17850337
hgdprs17850337
ensemblrs17850337
gopubmedrs17850337
geneviewrs17850337
scholarrs17850337
googlers17850337
pharmgkbrs17850337
gwascentralrs17850337
openSNPrs17850337
23andMers17850337
23andMe allrs17850337
SNP Nexus

SNPshotrs17850337
SNPdbers17850337
MSV3drs17850337
GWAS Ctlgrs17850337
Max Magnitude0
ClinVar
Risk rs17850337(A,C,G;A,C,G)
Alt rs17850337(A,C,G;A,C,G)
Reference rs17850337(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239011T>A; NC_000006.11:g.31239011T>C
CLNSRC
CLNACC