rs267606873

Orientation

minus

Stabilized

minus

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

Make rs267606873(A;A)

Make rs267606873(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

219057627

Gene

IHH

is a	snp
is	mentioned by
dbSNP	rs267606873
dbSNP (classic)	rs267606873
ClinGen	rs267606873
ebi	rs267606873
HLI	rs267606873
Exac	rs267606873
Gnomad	rs267606873
Varsome	rs267606873
LitVar	rs267606873
Map	rs267606873
PheGenI	rs267606873
Biobank	rs267606873
1000 genomes	rs267606873
hgdp	rs267606873
ensembl	rs267606873
geneview	rs267606873
scholar	rs267606873
google	rs267606873
pharmgkb	rs267606873
gwascentral	rs267606873
openSNP	rs267606873
23andMe	rs267606873
SNPshot	rs267606873
SNPdbe	rs267606873
MSV3d	rs267606873
GWAS Ctlg	rs267606873

Max Magnitude

0

ClinVar
Risk	rs267606873(A;A)
Alt	rs267606873(A;A)
Reference	Rs267606873(G;G)
Significance	Pathogenic
Disease	Brachydactyly type A1
Variation	info
Gene	IHH
CLNDBN	Brachydactyly type A1
Reversed	1
HGVS	NC_000002.11:g.219922349C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009425.3,