Have questions? Visit https://www.reddit.com/r/SNPedia

rs199503269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199503269(A;A)
Make rs199503269(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position214937608
GeneABCA12, LOC101928103
is asnp
is mentioned by
dbSNPrs199503269
dbSNP (classic)rs199503269
ClinGenrs199503269
ebirs199503269
HLIrs199503269
Exacrs199503269
Gnomadrs199503269
Varsomers199503269
LitVarrs199503269
Maprs199503269
PheGenIrs199503269
Biobankrs199503269
1000 genomesrs199503269
hgdprs199503269
ensemblrs199503269
geneviewrs199503269
scholarrs199503269
googlers199503269
pharmgkbrs199503269
gwascentralrs199503269
openSNPrs199503269
23andMers199503269
23andMe allrs199503269
SNPshotrs199503269
SNPdbers199503269
MSV3drs199503269
GWAS Ctlgrs199503269
Max Magnitude0
ClinVar
Risk rs199503269(A;A)
Alt rs199503269(A;A)
Reference Rs199503269(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC101928103 ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215802332G>A
CLNSRC
CLNACC RCV000480311.1,