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rs387907215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907215(C;T)
Make rs387907215(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position68542796
GeneFAM20A, PRKAR1A
is asnp
is mentioned by
dbSNPrs387907215
ebirs387907215
HLIrs387907215
Exacrs387907215
Varsomers387907215
Maprs387907215
PheGenIrs387907215
hapmaprs387907215
1000 genomesrs387907215
hgdprs387907215
ensemblrs387907215
gopubmedrs387907215
geneviewrs387907215
scholarrs387907215
googlers387907215
pharmgkbrs387907215
gwascentralrs387907215
openSNPrs387907215
23andMers387907215
23andMe allrs387907215
SNP Nexus

SNPshotrs387907215
SNPdbers387907215
MSV3drs387907215
GWAS Ctlgrs387907215
Max Magnitude0
ClinVar
Risk rs387907215(T;T)
Alt rs387907215(T;T)
Reference rs387907215(C;C)
Significance Pathogenic
Disease Enamel-renal syndrome
Variation info
Gene PRKAR1A FAM20A
CLNDBN Enamel-renal syndrome
Reversed 1
HGVS NC_000017.10:g.66538937G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000029154.4,