rs387907325

Orientation

plus

Stabilized

plus

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

Make rs387907325(-;T)

Make rs387907325(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

41819560

Gene

FKBP10

is a	snp
is	mentioned by
dbSNP	rs387907325
dbSNP (classic)	rs387907325
ClinGen	rs387907325
ebi	rs387907325
HLI	rs387907325
Exac	rs387907325
Gnomad	rs387907325
Varsome	rs387907325
LitVar	rs387907325
Map	rs387907325
PheGenI	rs387907325
Biobank	rs387907325
1000 genomes	rs387907325
hgdp	rs387907325
ensembl	rs387907325
geneview	rs387907325
scholar	rs387907325
google	rs387907325
pharmgkb	rs387907325
gwascentral	rs387907325
openSNP	rs387907325
23andMe	rs387907325
SNPshot	rs387907325
SNPdbe	rs387907325
MSV3d	rs387907325
GWAS Ctlg	rs387907325

Max Magnitude

0

ClinVar
Risk	rs387907325(T;T)
Alt	rs387907325(T;T)
Reference	Rs387907325(-;-)
Significance	Pathogenic
Disease	Osteogenesis imperfecta type 12
Variation	info
Gene	FKBP10
CLNDBN	Osteogenesis imperfecta type 12
Reversed	0
HGVS	NC_000017.10:g.39975812dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000034825.7,