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rs17879195

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17879195(A;A)
Make rs17879195(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271528
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17879195
ebirs17879195
HLIrs17879195
Exacrs17879195
Varsomers17879195
Maprs17879195
PheGenIrs17879195
hapmaprs17879195
1000 genomesrs17879195
hgdprs17879195
ensemblrs17879195
gopubmedrs17879195
geneviewrs17879195
scholarrs17879195
googlers17879195
pharmgkbrs17879195
gwascentralrs17879195
openSNPrs17879195
23andMers17879195
23andMe allrs17879195
SNP Nexus

SNPshotrs17879195
SNPdbers17879195
MSV3drs17879195
GWAS Ctlgrs17879195
GMAF0.213
Max Magnitude0
ClinVar
Risk rs17879195(A;A)
Alt rs17879195(A;A)
Reference rs17879195(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239305C>T
CLNSRC
CLNACC