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rs142534126

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142534126(C;T)
Make rs142534126(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position113345961
GeneANK2
is asnp
is mentioned by
dbSNPrs142534126
ebirs142534126
HLIrs142534126
Exacrs142534126
Varsomers142534126
Maprs142534126
PheGenIrs142534126
hapmaprs142534126
1000 genomesrs142534126
hgdprs142534126
ensemblrs142534126
gopubmedrs142534126
geneviewrs142534126
scholarrs142534126
googlers142534126
pharmgkbrs142534126
gwascentralrs142534126
openSNPrs142534126
23andMers142534126
23andMe allrs142534126
SNP Nexus

SNPshotrs142534126
SNPdbers142534126
MSV3drs142534126
GWAS Ctlgrs142534126
Max Magnitude0
ClinVar
Risk rs142534126(T;T)
Alt rs142534126(T;T)
Reference rs142534126(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANK2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.114267117C>T
CLNSRC
CLNACC RCV000170701.3,