rs121918347

Orientation

plus

Stabilized

plus

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

Make rs121918347(G;T)

Make rs121918347(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

129210500

Gene

SMO

is a	snp
is	mentioned by
dbSNP	rs121918347
dbSNP (classic)	rs121918347
ClinGen	rs121918347
ebi	rs121918347
HLI	rs121918347
Exac	rs121918347
Gnomad	rs121918347
Varsome	rs121918347
LitVar	rs121918347
Map	rs121918347
PheGenI	rs121918347
Biobank	rs121918347
1000 genomes	rs121918347
hgdp	rs121918347
ensembl	rs121918347
geneview	rs121918347
scholar	rs121918347
google	rs121918347
pharmgkb	rs121918347
gwascentral	rs121918347
openSNP	rs121918347
23andMe	rs121918347
SNPshot	rs121918347
SNPdbe	rs121918347
MSV3d	rs121918347
GWAS Ctlg	rs121918347

Max Magnitude

0

OMIM	601500
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918347(T;T)
Alt	rs121918347(T;T)
Reference	Rs121918347(G;G)
Significance	Pathogenic
Disease	Basal cell carcinoma
Variation	info
Gene	SMO
CLNDBN	Basal cell carcinoma, somatic
Reversed	0
HGVS	NC_000007.13:g.128850341G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008586.5,