rs104894046

Orientation

minus

Stabilized

minus

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

Make rs104894046(G;T)

Make rs104894046(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

155803439

Gene

SHH

is a	snp
is	mentioned by
dbSNP	rs104894046
dbSNP (classic)	rs104894046
ClinGen	rs104894046
ebi	rs104894046
HLI	rs104894046
Exac	rs104894046
Gnomad	rs104894046
Varsome	rs104894046
LitVar	rs104894046
Map	rs104894046
PheGenI	rs104894046
Biobank	rs104894046
1000 genomes	rs104894046
hgdp	rs104894046
ensembl	rs104894046
geneview	rs104894046
scholar	rs104894046
google	rs104894046
pharmgkb	rs104894046
gwascentral	rs104894046
openSNP	rs104894046
23andMe	rs104894046
SNPshot	rs104894046
SNPdbe	rs104894046
MSV3d	rs104894046
GWAS Ctlg	rs104894046

Max Magnitude

0

OMIM	600725
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104894046(A;A) rs104894046(T;T)
Alt	rs104894046(A;A) rs104894046(T;T)
Reference	Rs104894046(G;G)
Significance	Pathogenic
Disease	Holoprosencephaly 3
Variation	info
Gene	SHH
CLNDBN	Holoprosencephaly 3
Reversed	1
HGVS	NC_000007.13:g.155596133C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009435.2,