rs869025223

Orientation

plus

Stabilized

plus

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

Make rs869025223(-;-)

Make rs869025223(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

41819588

Gene

FKBP10

is a	snp
is	mentioned by
dbSNP	rs869025223
dbSNP (classic)	rs869025223
ClinGen	rs869025223
ebi	rs869025223
HLI	rs869025223
Exac	rs869025223
Gnomad	rs869025223
Varsome	rs869025223
LitVar	rs869025223
Map	rs869025223
PheGenI	rs869025223
Biobank	rs869025223
1000 genomes	rs869025223
hgdp	rs869025223
ensembl	rs869025223
geneview	rs869025223
scholar	rs869025223
google	rs869025223
pharmgkb	rs869025223
gwascentral	rs869025223
openSNP	rs869025223
23andMe	rs869025223
SNPshot	rs869025223
SNPdbe	rs869025223
MSV3d	rs869025223
GWAS Ctlg	rs869025223

Max Magnitude

0

ClinVar
Risk	rs869025223(-;-)
Alt	rs869025223(-;-)
Reference	Rs869025223(A;A)
Significance	Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	FKBP10
CLNDBN	Osteogenesis imperfecta, type XI
Reversed	0
HGVS	NC_000017.10:g.39975840delA
CLNSRC
CLNACC	RCV000208538.2,