rs1064794260

Orientation

minus

Stabilized

minus

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

Chromosome

9

Position

95459654

Gene

PTCH1

is a	snp
is	mentioned by
dbSNP	rs1064794260
dbSNP (classic)	rs1064794260
ClinGen	rs1064794260
ebi	rs1064794260
HLI	rs1064794260
Exac	rs1064794260
Gnomad	rs1064794260
Varsome	rs1064794260
LitVar	rs1064794260
Map	rs1064794260
PheGenI	rs1064794260
Biobank	rs1064794260
1000 genomes	rs1064794260
hgdp	rs1064794260
ensembl	rs1064794260
geneview	rs1064794260
scholar	rs1064794260
google	rs1064794260
pharmgkb	rs1064794260
gwascentral	rs1064794260
openSNP	rs1064794260
23andMe	rs1064794260
SNPshot	rs1064794260
SNPdbe	rs1064794260
MSV3d	rs1064794260
GWAS Ctlg	rs1064794260

Max Magnitude

0

ClinVar
Risk	rs1064794260(T;T)
Alt	rs1064794260(T;T)
Reference	Rs1064794260(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTCH1
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000009.11:g.98221936G>A
CLNSRC
CLNACC	RCV000479378.1, RCV000492276.1,