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rs587776912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776912(C;C)
Make rs587776912(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position68542811
GeneFAM20A, PRKAR1A
is asnp
is mentioned by
dbSNPrs587776912
ebirs587776912
HLIrs587776912
Exacrs587776912
Varsomers587776912
Maprs587776912
PheGenIrs587776912
hapmaprs587776912
1000 genomesrs587776912
hgdprs587776912
ensemblrs587776912
gopubmedrs587776912
geneviewrs587776912
scholarrs587776912
googlers587776912
pharmgkbrs587776912
gwascentralrs587776912
openSNPrs587776912
23andMers587776912
23andMe allrs587776912
SNP Nexus

SNPshotrs587776912
SNPdbers587776912
MSV3drs587776912
GWAS Ctlgrs587776912
Max Magnitude0
ClinVar
Risk rs587776912(C;C)
Alt rs587776912(C;C)
Reference rs587776912(T;T)
Significance Pathogenic
Disease Enamel-renal syndrome
Variation info
Gene PRKAR1A FAM20A
CLNDBN Enamel-renal syndrome
Reversed 0
HGVS NC_000017.10:g.66538952T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029151.3,