rs769983049

Orientation

plus

Stabilized

plus

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

Make rs769983049(C;C)

Make rs769983049(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

171108154

Gene

FMO3

is a	snp
is	mentioned by
dbSNP	rs769983049
dbSNP (classic)	rs769983049
ClinGen	rs769983049
ebi	rs769983049
HLI	rs769983049
Exac	rs769983049
Gnomad	rs769983049
Varsome	rs769983049
LitVar	rs769983049
Map	rs769983049
PheGenI	rs769983049
Biobank	rs769983049
1000 genomes	rs769983049
hgdp	rs769983049
ensembl	rs769983049
geneview	rs769983049
scholar	rs769983049
google	rs769983049
pharmgkb	rs769983049
gwascentral	rs769983049
openSNP	rs769983049
23andMe	rs769983049
SNPshot	rs769983049
SNPdbe	rs769983049
MSV3d	rs769983049
GWAS Ctlg	rs769983049

Max Magnitude

0

ClinVar
Risk	rs769983049(C;C) rs769983049(G;G)
Alt	rs769983049(C;C) rs769983049(G;G)
Reference	Rs769983049(T;T)
Significance	Pathogenic
Disease	Trimethylaminuria
Variation	info
Gene	FMO3
CLNDBN	Trimethylaminuria
Reversed	0
HGVS	NC_000001.10:g.171077295T>C
CLNSRC
CLNACC	RCV000201278.1,