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rs587776911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(CTG;CTG) 0 common in clinvar
Make rs587776911(-;-)
Make rs587776911(-;AG)
ReferenceGRCh38 38.1/142
Chromosome17
Position68600632
GeneFAM20A
is asnp
is mentioned by
dbSNPrs587776911
ebirs587776911
HLIrs587776911
Exacrs587776911
Varsomers587776911
Maprs587776911
PheGenIrs587776911
hapmaprs587776911
1000 genomesrs587776911
hgdprs587776911
ensemblrs587776911
gopubmedrs587776911
geneviewrs587776911
scholarrs587776911
googlers587776911
pharmgkbrs587776911
gwascentralrs587776911
openSNPrs587776911
23andMers587776911
23andMe allrs587776911
SNP Nexus

SNPshotrs587776911
SNPdbers587776911
MSV3drs587776911
GWAS Ctlgrs587776911
Max Magnitude0
ClinVar
Risk rs587776911(AGG,G;AGG,G)
Alt rs587776911(AGG,G;AGG,G)
Reference rs587776911(CTG;CTG)
Significance Pathogenic
Disease Enamel-renal syndrome
Variation info
Gene FAM20A
CLNDBN Enamel-renal syndrome
Reversed 1
HGVS NC_000017.10:g.66596773_66596774delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000029150.5,