rs764125009

Orientation

plus

Stabilized

plus

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

Make rs764125009(G;T)

Make rs764125009(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

105601349

Gene

FKTN

is a	snp
is	mentioned by
dbSNP	rs764125009
dbSNP (classic)	rs764125009
ClinGen	rs764125009
ebi	rs764125009
HLI	rs764125009
Exac	rs764125009
Gnomad	rs764125009
Varsome	rs764125009
LitVar	rs764125009
Map	rs764125009
PheGenI	rs764125009
Biobank	rs764125009
1000 genomes	rs764125009
hgdp	rs764125009
ensembl	rs764125009
geneview	rs764125009
scholar	rs764125009
google	rs764125009
pharmgkb	rs764125009
gwascentral	rs764125009
openSNP	rs764125009
23andMe	rs764125009
SNPshot	rs764125009
SNPdbe	rs764125009
MSV3d	rs764125009
GWAS Ctlg	rs764125009

Max Magnitude

0

ClinVar
Risk	rs764125009(C;C) rs764125009(T;T)
Alt	rs764125009(C;C) rs764125009(T;T)
Reference	Rs764125009(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FKTN
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.108363630G>T
CLNSRC
CLNACC	RCV000224731.1,