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

rs587780305

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780305(A;A)
Make rs587780305(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position88805870
GeneCDT1
is asnp
is mentioned by
dbSNPrs587780305
ebirs587780305
HLIrs587780305
Exacrs587780305
Varsomers587780305
Maprs587780305
PheGenIrs587780305
hapmaprs587780305
1000 genomesrs587780305
hgdprs587780305
ensemblrs587780305
gopubmedrs587780305
geneviewrs587780305
scholarrs587780305
googlers587780305
pharmgkbrs587780305
gwascentralrs587780305
openSNPrs587780305
23andMers587780305
23andMe allrs587780305
SNP Nexus

SNPshotrs587780305
SNPdbers587780305
MSV3drs587780305
GWAS Ctlgrs587780305
Max Magnitude0
ClinVar
Risk rs587780305(A,T;A,T)
Alt rs587780305(A,T;A,T)
Reference rs587780305(G;G)
Significance Pathogenic
Disease Meier-Gorlin syndrome 4
Variation info
Gene CDT1
CLNDBN Meier-Gorlin syndrome 4
Reversed 0
HGVS NC_000016.9:g.88872278G>A
CLNSRC
CLNACC RCV000116636.1,