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rs587776914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776914(C;C)
Make rs587776914(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position68554829
GeneFAM20A
is asnp
is mentioned by
dbSNPrs587776914
ebirs587776914
HLIrs587776914
Exacrs587776914
Varsomers587776914
Maprs587776914
PheGenIrs587776914
hapmaprs587776914
1000 genomesrs587776914
hgdprs587776914
ensemblrs587776914
gopubmedrs587776914
geneviewrs587776914
scholarrs587776914
googlers587776914
pharmgkbrs587776914
gwascentralrs587776914
openSNPrs587776914
23andMers587776914
23andMe allrs587776914
SNP Nexus

SNPshotrs587776914
SNPdbers587776914
MSV3drs587776914
GWAS Ctlgrs587776914
Max Magnitude0
ClinVar
Risk rs587776914(C,T;C,T)
Alt rs587776914(C,T;C,T)
Reference rs587776914(A;A)
Significance Pathogenic
Disease Enamel-renal syndrome
Variation info
Gene FAM20A
CLNDBN Enamel-renal syndrome
Reversed 1
HGVS NC_000017.10:g.66550970T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029153.4,