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rs41544416

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544416(C;T)
Make rs41544416(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270587
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544416
ebirs41544416
HLIrs41544416
Exacrs41544416
Varsomers41544416
Maprs41544416
PheGenIrs41544416
hapmaprs41544416
1000 genomesrs41544416
hgdprs41544416
ensemblrs41544416
gopubmedrs41544416
geneviewrs41544416
scholarrs41544416
googlers41544416
pharmgkbrs41544416
gwascentralrs41544416
openSNPrs41544416
23andMers41544416
23andMe allrs41544416
SNP Nexus

SNPshotrs41544416
SNPdbers41544416
MSV3drs41544416
GWAS Ctlgrs41544416
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs41544416(T;T)
Alt rs41544416(T;T)
Reference rs41544416(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238364G>A
CLNSRC
CLNACC