rs730880965

Orientation

minus

Stabilized

minus

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

Make rs730880965(A;A)

Make rs730880965(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

114713915

Gene

NRAS

is a	snp
is	mentioned by
dbSNP	rs730880965
dbSNP (classic)	rs730880965
ClinGen	rs730880965
ebi	rs730880965
HLI	rs730880965
Exac	rs730880965
Gnomad	rs730880965
Varsome	rs730880965
LitVar	rs730880965
Map	rs730880965
PheGenI	rs730880965
Biobank	rs730880965
1000 genomes	rs730880965
hgdp	rs730880965
ensembl	rs730880965
geneview	rs730880965
scholar	rs730880965
google	rs730880965
pharmgkb	rs730880965
gwascentral	rs730880965
openSNP	rs730880965
23andMe	rs730880965
SNPshot	rs730880965
SNPdbe	rs730880965
MSV3d	rs730880965
GWAS Ctlg	rs730880965

Max Magnitude

0

ClinVar
Risk	rs730880965(A;A)
Alt	rs730880965(A;A)
Reference	Rs730880965(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NRAS
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.115256536C>T
CLNSRC
CLNACC	RCV000158981.1,