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rs41542217

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41542217(A;C)
Make rs41542217(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270333
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41542217
ebirs41542217
HLIrs41542217
Exacrs41542217
Varsomers41542217
Maprs41542217
PheGenIrs41542217
hapmaprs41542217
1000 genomesrs41542217
hgdprs41542217
ensemblrs41542217
gopubmedrs41542217
geneviewrs41542217
scholarrs41542217
googlers41542217
pharmgkbrs41542217
gwascentralrs41542217
openSNPrs41542217
23andMers41542217
23andMe allrs41542217
SNP Nexus

SNPshotrs41542217
SNPdbers41542217
MSV3drs41542217
GWAS Ctlgrs41542217
Max Magnitude0
ClinVar
Risk rs41542217(C;C)
Alt rs41542217(C;C)
Reference rs41542217(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238110T>G
CLNSRC
CLNACC