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rs755391236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs755391236(C;C)
Make rs755391236(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position214997733
GeneABCA12
is asnp
is mentioned by
dbSNPrs755391236
dbSNP (classic)rs755391236
ClinGenrs755391236
ebirs755391236
HLIrs755391236
Exacrs755391236
Gnomadrs755391236
Varsomers755391236
LitVarrs755391236
Maprs755391236
PheGenIrs755391236
Biobankrs755391236
1000 genomesrs755391236
hgdprs755391236
ensemblrs755391236
geneviewrs755391236
scholarrs755391236
googlers755391236
pharmgkbrs755391236
gwascentralrs755391236
openSNPrs755391236
23andMers755391236
23andMe allrs755391236
SNPshotrs755391236
SNPdbers755391236
MSV3drs755391236
GWAS Ctlgrs755391236
Max Magnitude0
ClinVar
Risk rs755391236(A;A) rs755391236(C;C)
Alt rs755391236(A;A) rs755391236(C;C)
Reference Rs755391236(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215862457T>A
CLNSRC
CLNACC RCV000254841.1,