rs137853215

Orientation

plus

Stabilized

plus

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

Make rs137853215(A;G)

Make rs137853215(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

87349309

Gene	CCNH, RASA1

is a	snp
is	mentioned by
dbSNP	rs137853215
dbSNP (classic)	rs137853215
ClinGen	rs137853215
ebi	rs137853215
HLI	rs137853215
Exac	rs137853215
Gnomad	rs137853215
Varsome	rs137853215
LitVar	rs137853215
Map	rs137853215
PheGenI	rs137853215
Biobank	rs137853215
1000 genomes	rs137853215
hgdp	rs137853215
ensembl	rs137853215
geneview	rs137853215
scholar	rs137853215
google	rs137853215
pharmgkb	rs137853215
gwascentral	rs137853215
openSNP	rs137853215
23andMe	rs137853215
SNPshot	rs137853215
SNPdbe	rs137853215
MSV3d	rs137853215
GWAS Ctlg	rs137853215

Max Magnitude

0

OMIM	139150
Desc
Variant	0002
Related	also

ClinVar
Risk	rs137853215(G;G)
Alt	rs137853215(G;G)
Reference	Rs137853215(A;A)
Significance	Pathogenic
Disease	Basal cell carcinoma
Variation	info
Gene	RASA1
CLNDBN	Basal cell carcinoma, somatic
Reversed	0
HGVS	NC_000005.9:g.86645126A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017368.4,