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rs587777531

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(CT;CT) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777531(-;-)
Make rs587777531(-;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position68554805
GeneFAM20A
is asnp
is mentioned by
dbSNPrs587777531
dbSNP (old)rs587777531
ClinGenrs587777531
ebirs587777531
HLIrs587777531
Exacrs587777531
Gnomadrs587777531
Varsomers587777531
Maprs587777531
PheGenIrs587777531
Biobankrs587777531
1000 genomesrs587777531
hgdprs587777531
ensemblrs587777531
gopubmedrs587777531
geneviewrs587777531
scholarrs587777531
googlers587777531
pharmgkbrs587777531
gwascentralrs587777531
openSNPrs587777531
23andMers587777531
23andMe allrs587777531
SNP Nexus

SNPshotrs587777531
SNPdbers587777531
MSV3drs587777531
GWAS Ctlgrs587777531
Max Magnitude0
ClinVar
Risk Rs587777531(G;G) rs587777531(-;-)
Alt Rs587777531(G;G) rs587777531(-;-)
Reference Rs587777531(C;C)
Significance Pathogenic
Disease Enamel-renal syndrome
Variation info
Gene FAM20A
CLNDBN Enamel-renal syndrome
Reversed 1
HGVS NC_000017.10:g.66550946delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000128614.3,