rs730880967

Orientation

minus

Stabilized

minus

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

Make rs730880967(-;GGA)

Make rs730880967(GGA;GGA)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

114713976

Gene

NRAS

is a	snp
is	mentioned by
dbSNP	rs730880967
dbSNP (classic)	rs730880967
ClinGen	rs730880967
ebi	rs730880967
HLI	rs730880967
Exac	rs730880967
Gnomad	rs730880967
Varsome	rs730880967
LitVar	rs730880967
Map	rs730880967
PheGenI	rs730880967
Biobank	rs730880967
1000 genomes	rs730880967
hgdp	rs730880967
ensembl	rs730880967
geneview	rs730880967
scholar	rs730880967
google	rs730880967
pharmgkb	rs730880967
gwascentral	rs730880967
openSNP	rs730880967
23andMe	rs730880967
SNPshot	rs730880967
SNPdbe	rs730880967
MSV3d	rs730880967
GWAS Ctlg	rs730880967

Max Magnitude

0

ClinVar
Risk	rs730880967(GGA;GGA)
Alt	rs730880967(GGA;GGA)
Reference	Rs730880967(-;-)
Significance	Pathogenic
Disease	Rasopathy
Variation	info
Gene	NRAS
CLNDBN	Rasopathy
Reversed	1
HGVS	NC_000001.10:g.115256598_115256600dupTCC
CLNSRC
CLNACC	RCV000158984.1,