rs137853341

Orientation

minus

Stabilized

minus

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

Make rs137853341(A;A)

Make rs137853341(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

155803142

Gene

SHH

is a	snp
is	mentioned by
dbSNP	rs137853341
dbSNP (classic)	rs137853341
ClinGen	rs137853341
ebi	rs137853341
HLI	rs137853341
Exac	rs137853341
Gnomad	rs137853341
Varsome	rs137853341
LitVar	rs137853341
Map	rs137853341
PheGenI	rs137853341
Biobank	rs137853341
1000 genomes	rs137853341
hgdp	rs137853341
ensembl	rs137853341
geneview	rs137853341
scholar	rs137853341
google	rs137853341
pharmgkb	rs137853341
gwascentral	rs137853341
openSNP	rs137853341
23andMe	rs137853341
SNPshot	rs137853341
SNPdbe	rs137853341
MSV3d	rs137853341
GWAS Ctlg	rs137853341

Max Magnitude

0

OMIM	600725
Desc
Variant	0010
Related	also

ClinVar
Risk	rs137853341(A;A)
Alt	rs137853341(A;A)
Reference	Rs137853341(G;G)
Significance	Pathogenic
Disease	Holoprosencephaly 3
Variation	info
Gene	SHH
CLNDBN	Holoprosencephaly 3
Reversed	1
HGVS	NC_000007.13:g.155595836C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009436.2,