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rs41563215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41563215(C;C)
Make rs41563215(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270735
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41563215
ebirs41563215
HLIrs41563215
Exacrs41563215
Varsomers41563215
Maprs41563215
PheGenIrs41563215
hapmaprs41563215
1000 genomesrs41563215
hgdprs41563215
ensemblrs41563215
gopubmedrs41563215
geneviewrs41563215
scholarrs41563215
googlers41563215
pharmgkbrs41563215
gwascentralrs41563215
openSNPrs41563215
23andMers41563215
23andMe allrs41563215
SNP Nexus

SNPshotrs41563215
SNPdbers41563215
MSV3drs41563215
GWAS Ctlgrs41563215
Max Magnitude0
ClinVar
Risk rs41563215(C;C)
Alt rs41563215(C;C)
Reference rs41563215(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238512A>G
CLNSRC
CLNACC