rs730880461

Orientation

minus

Stabilized

minus

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

Make rs730880461(A;A)

Make rs730880461(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

533853

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs730880461
dbSNP (classic)	rs730880461
ClinGen	rs730880461
ebi	rs730880461
HLI	rs730880461
Exac	rs730880461
Gnomad	rs730880461
Varsome	rs730880461
LitVar	rs730880461
Map	rs730880461
PheGenI	rs730880461
Biobank	rs730880461
1000 genomes	rs730880461
hgdp	rs730880461
ensembl	rs730880461
geneview	rs730880461
scholar	rs730880461
google	rs730880461
pharmgkb	rs730880461
gwascentral	rs730880461
openSNP	rs730880461
23andMe	rs730880461
SNPshot	rs730880461
SNPdbe	rs730880461
MSV3d	rs730880461
GWAS Ctlg	rs730880461

Max Magnitude

0

ClinVar
Risk	rs730880461(A;A)
Alt	rs730880461(A;A)
Reference	Rs730880461(G;G)
Significance	Probable-Pathogenic
Disease	Rasopathy
Variation	info
Gene	HRAS
CLNDBN	Rasopathy
Reversed	1
HGVS	NC_000011.9:g.533853C>T
CLNSRC
CLNACC	RCV000157919.1,