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rs78897778

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs78897778(A;G)
Make rs78897778(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271220
GeneHLA-C
is asnp
is mentioned by
dbSNPrs78897778
ebirs78897778
HLIrs78897778
Exacrs78897778
Varsomers78897778
Maprs78897778
PheGenIrs78897778
hapmaprs78897778
1000 genomesrs78897778
hgdprs78897778
ensemblrs78897778
gopubmedrs78897778
geneviewrs78897778
scholarrs78897778
googlers78897778
pharmgkbrs78897778
gwascentralrs78897778
openSNPrs78897778
23andMers78897778
23andMe allrs78897778
SNP Nexus

SNPshotrs78897778
SNPdbers78897778
MSV3drs78897778
GWAS Ctlgrs78897778
Max Magnitude0
ClinVar
Risk rs78897778(G;G)
Alt rs78897778(G;G)
Reference rs78897778(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238997T>C
CLNSRC
CLNACC