rs387907354

Orientation

plus

Stabilized

plus

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

Make rs387907354(A;G)

Make rs387907354(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

48980693

Gene

WNT1

is a	snp
is	mentioned by
dbSNP	rs387907354
dbSNP (classic)	rs387907354
ClinGen	rs387907354
ebi	rs387907354
HLI	rs387907354
Exac	rs387907354
Gnomad	rs387907354
Varsome	rs387907354
LitVar	rs387907354
Map	rs387907354
PheGenI	rs387907354
Biobank	rs387907354
1000 genomes	rs387907354
hgdp	rs387907354
ensembl	rs387907354
geneview	rs387907354
scholar	rs387907354
google	rs387907354
pharmgkb	rs387907354
gwascentral	rs387907354
openSNP	rs387907354
23andMe	rs387907354
SNPshot	rs387907354
SNPdbe	rs387907354
MSV3d	rs387907354
GWAS Ctlg	rs387907354

Max Magnitude

0

ClinVar
Risk	rs387907354(G;G)
Alt	rs387907354(G;G)
Reference	Rs387907354(A;A)
Significance	Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	WNT1
CLNDBN	Osteogenesis imperfecta, type xv
Reversed	0
HGVS	NC_000012.11:g.49374476A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043493.28,