rs587776914

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0	common in clinvar

Make rs587776914(C;C)

Make rs587776914(C;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

68554829

Gene

FAM20A

is a	snp
is	mentioned by
dbSNP	rs587776914
dbSNP (classic)	rs587776914
ClinGen	rs587776914
ebi	rs587776914
HLI	rs587776914
Exac	rs587776914
Gnomad	rs587776914
Varsome	rs587776914
LitVar	rs587776914
Map	rs587776914
PheGenI	rs587776914
Biobank	rs587776914
1000 genomes	rs587776914
hgdp	rs587776914
ensembl	rs587776914
geneview	rs587776914
scholar	rs587776914
google	rs587776914
pharmgkb	rs587776914
gwascentral	rs587776914
openSNP	rs587776914
23andMe	rs587776914
SNPshot	rs587776914
SNPdbe	rs587776914
MSV3d	rs587776914
GWAS Ctlg	rs587776914

Max Magnitude

0

ClinVar
Risk	rs587776914(C;C) Rs587776914(T;T)
Alt	rs587776914(C;C) Rs587776914(T;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,