rs730880464

Orientation

minus

Stabilized

minus

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

Make rs730880464(C;C)

Make rs730880464(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

533535

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs730880464
dbSNP (classic)	rs730880464
ClinGen	rs730880464
ebi	rs730880464
HLI	rs730880464
Exac	rs730880464
Gnomad	rs730880464
Varsome	rs730880464
LitVar	rs730880464
Map	rs730880464
PheGenI	rs730880464
Biobank	rs730880464
1000 genomes	rs730880464
hgdp	rs730880464
ensembl	rs730880464
geneview	rs730880464
scholar	rs730880464
google	rs730880464
pharmgkb	rs730880464
gwascentral	rs730880464
openSNP	rs730880464
23andMe	rs730880464
SNPshot	rs730880464
SNPdbe	rs730880464
MSV3d	rs730880464
GWAS Ctlg	rs730880464

Max Magnitude

0

ClinVar
Risk	rs730880464(C;C)
Alt	rs730880464(C;C)
Reference	Rs730880464(G;G)
Significance	Probable-Pathogenic
Disease	Rasopathy
Variation	info
Gene	HRAS
CLNDBN	Rasopathy
Reversed	1
HGVS	NC_000011.9:g.533535C>G
CLNSRC
CLNACC	RCV000157923.1,