rs267606872

Orientation

minus

Stabilized

minus

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

Make rs267606872(A;A)

Make rs267606872(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

219057621

Gene

IHH

is a	snp
is	mentioned by
dbSNP	rs267606872
dbSNP (classic)	rs267606872
ClinGen	rs267606872
ebi	rs267606872
HLI	rs267606872
Exac	rs267606872
Gnomad	rs267606872
Varsome	rs267606872
LitVar	rs267606872
Map	rs267606872
PheGenI	rs267606872
Biobank	rs267606872
1000 genomes	rs267606872
hgdp	rs267606872
ensembl	rs267606872
geneview	rs267606872
scholar	rs267606872
google	rs267606872
pharmgkb	rs267606872
gwascentral	rs267606872
openSNP	rs267606872
23andMe	rs267606872
SNPshot	rs267606872
SNPdbe	rs267606872
MSV3d	rs267606872
GWAS Ctlg	rs267606872

Max Magnitude

0

ClinVar
Risk	rs267606872(A;A)
Alt	rs267606872(A;A)
Reference	Rs267606872(C;C)
Significance	Pathogenic
Disease	Brachydactyly type A1
Variation	info
Gene	IHH
CLNDBN	Brachydactyly type A1
Reversed	1
HGVS	NC_000002.11:g.219922343G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009426.2,