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rs41550315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41550315(A;A)
Make rs41550315(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31269487
is asnp
is mentioned by
dbSNPrs41550315
dbSNP (old)rs41550315
ClinGenrs41550315
ebirs41550315
HLIrs41550315
Exacrs41550315
Gnomadrs41550315
Varsomers41550315
Maprs41550315
PheGenIrs41550315
Biobankrs41550315
1000 genomesrs41550315
hgdprs41550315
ensemblrs41550315
gopubmedrs41550315
geneviewrs41550315
scholarrs41550315
googlers41550315
pharmgkbrs41550315
gwascentralrs41550315
openSNPrs41550315
23andMers41550315
23andMe allrs41550315
SNP Nexus

SNPshotrs41550315
SNPdbers41550315
MSV3drs41550315
GWAS Ctlgrs41550315
Max Magnitude0
ClinVar
Risk rs41550315(A;A)
Alt rs41550315(A;A)
Reference Rs41550315(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237265C>T
CLNSRC
CLNACC