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

rs114863111

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs114863111(A;A)
Make rs114863111(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position214987734
GeneABCA12
is asnp
is mentioned by
dbSNPrs114863111
dbSNP (old)rs114863111
ClinGenrs114863111
ebirs114863111
HLIrs114863111
Exacrs114863111
Gnomadrs114863111
Varsomers114863111
Maprs114863111
PheGenIrs114863111
Biobankrs114863111
1000 genomesrs114863111
hgdprs114863111
ensemblrs114863111
gopubmedrs114863111
geneviewrs114863111
scholarrs114863111
googlers114863111
pharmgkbrs114863111
gwascentralrs114863111
openSNPrs114863111
23andMers114863111
23andMe allrs114863111
SNPshotrs114863111
SNPdbers114863111
MSV3drs114863111
GWAS Ctlgrs114863111
Max Magnitude0
ClinVar
Risk rs114863111(A;A) rs114863111(T;T)
Alt rs114863111(A;A) rs114863111(T;T)
Reference Rs114863111(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215852458G>A
CLNSRC
CLNACC RCV000255106.1,