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rs147941846

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147941846(C;T)
Make rs147941846(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position115768448
GeneCASQ2
is asnp
is mentioned by
dbSNPrs147941846
ebirs147941846
HLIrs147941846
Exacrs147941846
Varsomers147941846
Maprs147941846
PheGenIrs147941846
hapmaprs147941846
1000 genomesrs147941846
hgdprs147941846
ensemblrs147941846
gopubmedrs147941846
geneviewrs147941846
scholarrs147941846
googlers147941846
pharmgkbrs147941846
gwascentralrs147941846
openSNPrs147941846
23andMers147941846
23andMe allrs147941846
SNP Nexus

SNPshotrs147941846
SNPdbers147941846
MSV3drs147941846
GWAS Ctlgrs147941846
Max Magnitude0
ClinVar
Risk rs147941846(T;T)
Alt rs147941846(T;T)
Reference rs147941846(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASQ2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.116311069C>T
CLNSRC
CLNACC RCV000170899.2,