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rs41548520

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41548520(A;A)
Make rs41548520(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271345
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41548520
ebirs41548520
HLIrs41548520
Exacrs41548520
Varsomers41548520
Maprs41548520
PheGenIrs41548520
hapmaprs41548520
1000 genomesrs41548520
hgdprs41548520
ensemblrs41548520
gopubmedrs41548520
geneviewrs41548520
scholarrs41548520
googlers41548520
pharmgkbrs41548520
gwascentralrs41548520
openSNPrs41548520
23andMers41548520
23andMe allrs41548520
SNP Nexus

SNPshotrs41548520
SNPdbers41548520
MSV3drs41548520
GWAS Ctlgrs41548520
Max Magnitude0
ClinVar
Risk rs41548520(A,G;A,G)
Alt rs41548520(A,G;A,G)
Reference rs41548520(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239122G>C; NC_000006.11:g.31239122G>T
CLNSRC
CLNACC