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rs1057521640

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521640(A;T)
Make rs1057521640(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position21861017
GeneABCC9
is asnp
is mentioned by
dbSNPrs1057521640
dbSNP (old)rs1057521640
ClinGenrs1057521640
ebirs1057521640
HLIrs1057521640
Exacrs1057521640
Gnomadrs1057521640
Varsomers1057521640
Maprs1057521640
PheGenIrs1057521640
Biobankrs1057521640
1000 genomesrs1057521640
hgdprs1057521640
ensemblrs1057521640
gopubmedrs1057521640
geneviewrs1057521640
scholarrs1057521640
googlers1057521640
pharmgkbrs1057521640
gwascentralrs1057521640
openSNPrs1057521640
23andMers1057521640
23andMe allrs1057521640
SNPshotrs1057521640
SNPdbers1057521640
MSV3drs1057521640
GWAS Ctlgrs1057521640
Max Magnitude0
ClinVar
Risk rs1057521640(T;T)
Alt rs1057521640(T;T)
Reference Rs1057521640(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.22013951T>A
CLNSRC
CLNACC RCV000441926.1,