Have questions? Visit https://www.reddit.com/r/SNPedia

rs41547914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41547914(A;A)
Make rs41547914(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943485
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41547914
ebirs41547914
HLIrs41547914
Exacrs41547914
Varsomers41547914
Maprs41547914
PheGenIrs41547914
hapmaprs41547914
1000 genomesrs41547914
hgdprs41547914
ensemblrs41547914
gopubmedrs41547914
geneviewrs41547914
scholarrs41547914
googlers41547914
pharmgkbrs41547914
gwascentralrs41547914
openSNPrs41547914
23andMers41547914
23andMe allrs41547914
SNP Nexus

SNPshotrs41547914
SNPdbers41547914
MSV3drs41547914
GWAS Ctlgrs41547914
Max Magnitude0
ClinVar
Risk rs41547914(A,C,T;A,C,T)
Alt rs41547914(A,C,T;A,C,T)
Reference rs41547914(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911262G>A; NC_000006.11:g.29911262G>C; NC_000006.11:g.29911262G>T
CLNSRC
CLNACC