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rs17879162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17879162(A;A)
Make rs17879162(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269480
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17879162
ebirs17879162
HLIrs17879162
Exacrs17879162
Varsomers17879162
Maprs17879162
PheGenIrs17879162
hapmaprs17879162
1000 genomesrs17879162
hgdprs17879162
ensemblrs17879162
gopubmedrs17879162
geneviewrs17879162
scholarrs17879162
googlers17879162
pharmgkbrs17879162
gwascentralrs17879162
openSNPrs17879162
23andMers17879162
23andMe allrs17879162
SNP Nexus

SNPshotrs17879162
SNPdbers17879162
MSV3drs17879162
GWAS Ctlgrs17879162
GMAF0.05005
Max Magnitude0
ClinVar
Risk rs17879162(A;A)
Alt rs17879162(A;A)
Reference rs17879162(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237257C>T
CLNSRC
CLNACC