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

rs797045946

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045946(A;G)
Make rs797045946(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position243270976
GeneSDCCAG8
is asnp
is mentioned by
dbSNPrs797045946
ebirs797045946
HLIrs797045946
Exacrs797045946
Varsomers797045946
Maprs797045946
PheGenIrs797045946
hapmaprs797045946
1000 genomesrs797045946
hgdprs797045946
ensemblrs797045946
gopubmedrs797045946
geneviewrs797045946
scholarrs797045946
googlers797045946
pharmgkbrs797045946
gwascentralrs797045946
openSNPrs797045946
23andMers797045946
23andMe allrs797045946
SNP Nexus

SNPshotrs797045946
SNPdbers797045946
MSV3drs797045946
GWAS Ctlgrs797045946
Max Magnitude0
ClinVar
Risk rs797045946(G;G)
Alt rs797045946(G;G)
Reference rs797045946(A;A)
Significance Pathogenic
Disease Senior-Loken syndrome 7
Variation info
Gene SDCCAG8
CLNDBN Senior-Loken syndrome 7
Reversed 0
HGVS NC_000001.10:g.243434278A>G
CLNSRC
CLNACC RCV000194923.1,