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rs767707248

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767707248(A;A)
Make rs767707248(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position215064205
GeneABCA12
is asnp
is mentioned by
dbSNPrs767707248
dbSNP (classic)rs767707248
ClinGenrs767707248
ebirs767707248
HLIrs767707248
Exacrs767707248
Gnomadrs767707248
Varsomers767707248
LitVarrs767707248
Maprs767707248
PheGenIrs767707248
Biobankrs767707248
1000 genomesrs767707248
hgdprs767707248
ensemblrs767707248
geneviewrs767707248
scholarrs767707248
googlers767707248
pharmgkbrs767707248
gwascentralrs767707248
openSNPrs767707248
23andMers767707248
23andMe allrs767707248
SNPshotrs767707248
SNPdbers767707248
MSV3drs767707248
GWAS Ctlgrs767707248
Max Magnitude0
ClinVar
Risk rs767707248(A;A)
Alt rs767707248(A;A)
Reference Rs767707248(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215928928G>A
CLNSRC
CLNACC RCV000255481.1,