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rs1057521820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521820(G;G)
Make rs1057521820(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position21807388
GeneABCC9, LOC105369689
is asnp
is mentioned by
dbSNPrs1057521820
dbSNP (old)rs1057521820
ClinGenrs1057521820
ebirs1057521820
HLIrs1057521820
Exacrs1057521820
Gnomadrs1057521820
Varsomers1057521820
LitVarrs1057521820
Maprs1057521820
PheGenIrs1057521820
Biobankrs1057521820
1000 genomesrs1057521820
hgdprs1057521820
ensemblrs1057521820
gopubmedrs1057521820
geneviewrs1057521820
scholarrs1057521820
googlers1057521820
pharmgkbrs1057521820
gwascentralrs1057521820
openSNPrs1057521820
23andMers1057521820
23andMe allrs1057521820
SNPshotrs1057521820
SNPdbers1057521820
MSV3drs1057521820
GWAS Ctlgrs1057521820
Max Magnitude0
ClinVar
Risk rs1057521820(G;G)
Alt rs1057521820(G;G)
Reference Rs1057521820(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21960322A>C
CLNSRC
CLNACC RCV000426029.1,