rs387907355

Orientation

plus

Stabilized

plus

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

Make rs387907355(G;T)

Make rs387907355(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

48980630

Gene

WNT1

is a	snp
is	mentioned by
dbSNP	rs387907355
dbSNP (classic)	rs387907355
ClinGen	rs387907355
ebi	rs387907355
HLI	rs387907355
Exac	rs387907355
Gnomad	rs387907355
Varsome	rs387907355
LitVar	rs387907355
Map	rs387907355
PheGenI	rs387907355
Biobank	rs387907355
1000 genomes	rs387907355
hgdp	rs387907355
ensembl	rs387907355
geneview	rs387907355
scholar	rs387907355
google	rs387907355
pharmgkb	rs387907355
gwascentral	rs387907355
openSNP	rs387907355
23andMe	rs387907355
SNPshot	rs387907355
SNPdbe	rs387907355
MSV3d	rs387907355
GWAS Ctlg	rs387907355

Max Magnitude

0

ClinVar
Risk	rs387907355(A;A) rs387907355(T;T)
Alt	rs387907355(A;A) rs387907355(T;T)
Reference	Rs387907355(G;G)
Significance	Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	WNT1
CLNDBN	Osteogenesis imperfecta, type xv
Reversed	0
HGVS	NC_000012.11:g.49374413G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043494.28,