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rs763481375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763481375(A;A)
Make rs763481375(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position215011631
GeneABCA12
is asnp
is mentioned by
dbSNPrs763481375
dbSNP (classic)rs763481375
ClinGenrs763481375
ebirs763481375
HLIrs763481375
Exacrs763481375
Gnomadrs763481375
Varsomers763481375
LitVarrs763481375
Maprs763481375
PheGenIrs763481375
Biobankrs763481375
1000 genomesrs763481375
hgdprs763481375
ensemblrs763481375
geneviewrs763481375
scholarrs763481375
googlers763481375
pharmgkbrs763481375
gwascentralrs763481375
openSNPrs763481375
23andMers763481375
23andMe allrs763481375
SNPshotrs763481375
SNPdbers763481375
MSV3drs763481375
GWAS Ctlgrs763481375
Max Magnitude0
ClinVar
Risk rs763481375(A;A)
Alt rs763481375(A;A)
Reference Rs763481375(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215876355G>A
CLNSRC
CLNACC RCV000256167.1,