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rs797045947

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045947(C;T)
Make rs797045947(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position243286332
GeneSDCCAG8
is asnp
is mentioned by
dbSNPrs797045947
ebirs797045947
HLIrs797045947
Exacrs797045947
Varsomers797045947
Maprs797045947
PheGenIrs797045947
hapmaprs797045947
1000 genomesrs797045947
hgdprs797045947
ensemblrs797045947
gopubmedrs797045947
geneviewrs797045947
scholarrs797045947
googlers797045947
pharmgkbrs797045947
gwascentralrs797045947
openSNPrs797045947
23andMers797045947
23andMe allrs797045947
SNP Nexus

SNPshotrs797045947
SNPdbers797045947
MSV3drs797045947
GWAS Ctlgrs797045947
Max Magnitude0
ClinVar
Risk rs797045947(T;T)
Alt rs797045947(T;T)
Reference rs797045947(C;C)
Significance Pathogenic
Disease Senior-Loken syndrome 7
Variation info
Gene SDCCAG8
CLNDBN Senior-Loken syndrome 7
Reversed 0
HGVS NC_000001.10:g.243449634C>T
CLNSRC
CLNACC RCV000193333.1,