rs121918348

Orientation

plus

Stabilized

plus

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

Make rs121918348(A;A)

Make rs121918348(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

129210997

Gene

SMO

is a	snp
is	mentioned by
dbSNP	rs121918348
dbSNP (classic)	rs121918348
ClinGen	rs121918348
ebi	rs121918348
HLI	rs121918348
Exac	rs121918348
Gnomad	rs121918348
Varsome	rs121918348
LitVar	rs121918348
Map	rs121918348
PheGenI	rs121918348
Biobank	rs121918348
1000 genomes	rs121918348
hgdp	rs121918348
ensembl	rs121918348
geneview	rs121918348
scholar	rs121918348
google	rs121918348
pharmgkb	rs121918348
gwascentral	rs121918348
openSNP	rs121918348
23andMe	rs121918348
SNPshot	rs121918348
SNPdbe	rs121918348
MSV3d	rs121918348
GWAS Ctlg	rs121918348

Max Magnitude

0

OMIM	601500
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121918348(A;A)
Alt	rs121918348(A;A)
Reference	Rs121918348(G;G)
Significance	Pathogenic
Disease	Basal cell carcinoma
Variation	info
Gene	SMO
CLNDBN	Basal cell carcinoma, somatic
Reversed	0
HGVS	NC_000007.13:g.128850838G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008587.4,