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rs794728955

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728955(A;T)
Make rs794728955(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position21845685
GeneABCC9
is asnp
is mentioned by
dbSNPrs794728955
ebirs794728955
HLIrs794728955
Exacrs794728955
Varsomers794728955
Maprs794728955
PheGenIrs794728955
hapmaprs794728955
1000 genomesrs794728955
hgdprs794728955
ensemblrs794728955
gopubmedrs794728955
geneviewrs794728955
scholarrs794728955
googlers794728955
pharmgkbrs794728955
gwascentralrs794728955
openSNPrs794728955
23andMers794728955
23andMe allrs794728955
SNP Nexus

SNPshotrs794728955
SNPdbers794728955
MSV3drs794728955
GWAS Ctlgrs794728955
Max Magnitude0
ClinVar
Risk rs794728955(T;T)
Alt rs794728955(T;T)
Reference rs794728955(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21998619T>A
CLNSRC
CLNACC RCV000183234.1,