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rs761557390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs761557390(A;C)
Make rs761557390(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position214966945
GeneABCA12
is asnp
is mentioned by
dbSNPrs761557390
dbSNP (classic)rs761557390
ClinGenrs761557390
ebirs761557390
HLIrs761557390
Exacrs761557390
Gnomadrs761557390
Varsomers761557390
LitVarrs761557390
Maprs761557390
PheGenIrs761557390
Biobankrs761557390
1000 genomesrs761557390
hgdprs761557390
ensemblrs761557390
geneviewrs761557390
scholarrs761557390
googlers761557390
pharmgkbrs761557390
gwascentralrs761557390
openSNPrs761557390
23andMers761557390
23andMe allrs761557390
SNPshotrs761557390
SNPdbers761557390
MSV3drs761557390
GWAS Ctlgrs761557390
Max Magnitude0
ClinVar
Risk rs761557390(C;C)
Alt rs761557390(C;C)
Reference Rs761557390(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215831669A>C
CLNSRC
CLNACC RCV000276997.1,