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rs763182554

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs763182554(A;C)
Make rs763182554(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position215011969
GeneABCA12
is asnp
is mentioned by
dbSNPrs763182554
dbSNP (classic)rs763182554
ClinGenrs763182554
ebirs763182554
HLIrs763182554
Exacrs763182554
Gnomadrs763182554
Varsomers763182554
LitVarrs763182554
Maprs763182554
PheGenIrs763182554
Biobankrs763182554
1000 genomesrs763182554
hgdprs763182554
ensemblrs763182554
geneviewrs763182554
scholarrs763182554
googlers763182554
pharmgkbrs763182554
gwascentralrs763182554
openSNPrs763182554
23andMers763182554
23andMe allrs763182554
SNPshotrs763182554
SNPdbers763182554
MSV3drs763182554
GWAS Ctlgrs763182554
Max Magnitude0
ClinVar
Risk rs763182554(C;C) rs763182554(G;G)
Alt rs763182554(C;C) rs763182554(G;G)
Reference Rs763182554(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215876693A>C
CLNSRC
CLNACC RCV000428022.1,