rs137853216

Orientation

plus

Stabilized

plus

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

Make rs137853216(A;G)

Make rs137853216(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

87349312

Gene	CCNH, RASA1

is a	snp
is	mentioned by
dbSNP	rs137853216
dbSNP (classic)	rs137853216
ClinGen	rs137853216
ebi	rs137853216
HLI	rs137853216
Exac	rs137853216
Gnomad	rs137853216
Varsome	rs137853216
LitVar	rs137853216
Map	rs137853216
PheGenI	rs137853216
Biobank	rs137853216
1000 genomes	rs137853216
hgdp	rs137853216
ensembl	rs137853216
geneview	rs137853216
scholar	rs137853216
google	rs137853216
pharmgkb	rs137853216
gwascentral	rs137853216
openSNP	rs137853216
23andMe	rs137853216
SNPshot	rs137853216
SNPdbe	rs137853216
MSV3d	rs137853216
GWAS Ctlg	rs137853216

Merged from

Rs28932772

Max Magnitude

0

OMIM	139150
Desc
Variant	0003
Related	also

ClinVar
Risk	rs137853216(G;G)
Alt	rs137853216(G;G)
Reference	Rs137853216(A;A)
Significance	Pathogenic
Disease	Basal cell carcinoma
Variation	info
Gene	RASA1
CLNDBN	Basal cell carcinoma, somatic
Reversed	0
HGVS	NC_000005.9:g.86645129A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017369.4,