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rs794728975

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728975(C;T)
Make rs794728975(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position90912966
GeneANKRD1
is asnp
is mentioned by
dbSNPrs794728975
ebirs794728975
HLIrs794728975
Exacrs794728975
Varsomers794728975
Maprs794728975
PheGenIrs794728975
hapmaprs794728975
1000 genomesrs794728975
hgdprs794728975
ensemblrs794728975
gopubmedrs794728975
geneviewrs794728975
scholarrs794728975
googlers794728975
pharmgkbrs794728975
gwascentralrs794728975
openSNPrs794728975
23andMers794728975
23andMe allrs794728975
SNP Nexus

SNPshotrs794728975
SNPdbers794728975
MSV3drs794728975
GWAS Ctlgrs794728975
Max Magnitude0
ClinVar
Risk rs794728975(T;T)
Alt rs794728975(T;T)
Reference rs794728975(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANKRD1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.92672723G>A
CLNSRC
CLNACC RCV000183301.2,