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

rs786205530

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205530(C;T)
Make rs786205530(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position96761733
GeneCNNM4
is asnp
is mentioned by
dbSNPrs786205530
ebirs786205530
HLIrs786205530
Exacrs786205530
Varsomers786205530
Maprs786205530
PheGenIrs786205530
hapmaprs786205530
1000 genomesrs786205530
hgdprs786205530
ensemblrs786205530
gopubmedrs786205530
geneviewrs786205530
scholarrs786205530
googlers786205530
pharmgkbrs786205530
gwascentralrs786205530
openSNPrs786205530
23andMers786205530
23andMe allrs786205530
SNP Nexus

SNPshotrs786205530
SNPdbers786205530
MSV3drs786205530
GWAS Ctlgrs786205530
Max Magnitude0
ClinVar
Risk rs786205530(T;T)
Alt rs786205530(T;T)
Reference rs786205530(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNNM4
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.97427470C>T
CLNSRC
CLNACC RCV000171299.1,