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rs78691935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs78691935(A;A)
Make rs78691935(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943434
GeneHLA-A
is asnp
is mentioned by
dbSNPrs78691935
ebirs78691935
HLIrs78691935
Exacrs78691935
Varsomers78691935
Maprs78691935
PheGenIrs78691935
hapmaprs78691935
1000 genomesrs78691935
hgdprs78691935
ensemblrs78691935
gopubmedrs78691935
geneviewrs78691935
scholarrs78691935
googlers78691935
pharmgkbrs78691935
gwascentralrs78691935
openSNPrs78691935
23andMers78691935
23andMe allrs78691935
SNP Nexus

SNPshotrs78691935
SNPdbers78691935
MSV3drs78691935
GWAS Ctlgrs78691935
Max Magnitude0
ClinVar
Risk rs78691935(A,C;A,C)
Alt rs78691935(A,C;A,C)
Reference rs78691935(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911211G>A; NC_000006.11:g.29911211G>C
CLNSRC
CLNACC