rs797044852

Orientation

plus

Stabilized

plus

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

Make rs797044852(-;-)

Make rs797044852(-;TG)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

41821033

Gene

FKBP10

is a	snp
is	mentioned by
dbSNP	rs797044852
dbSNP (classic)	rs797044852
ClinGen	rs797044852
ebi	rs797044852
HLI	rs797044852
Exac	rs797044852
Gnomad	rs797044852
Varsome	rs797044852
LitVar	rs797044852
Map	rs797044852
PheGenI	rs797044852
Biobank	rs797044852
1000 genomes	rs797044852
hgdp	rs797044852
ensembl	rs797044852
geneview	rs797044852
scholar	rs797044852
google	rs797044852
pharmgkb	rs797044852
gwascentral	rs797044852
openSNP	rs797044852
23andMe	rs797044852
SNPshot	rs797044852
SNPdbe	rs797044852
MSV3d	rs797044852
GWAS Ctlg	rs797044852

Max Magnitude

0

ClinVar
Risk	rs797044852(-;-)
Alt	rs797044852(-;-)
Reference	Rs797044852(TG;TG)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	FKBP10
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000017.10:g.39977285_39977286delTG
CLNSRC
CLNACC	RCV000190651.1,