rs730880460

Orientation

minus

Stabilized

minus

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

Make rs730880460(A;A)

Make rs730880460(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

533877

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs730880460
dbSNP (classic)	rs730880460
ClinGen	rs730880460
ebi	rs730880460
HLI	rs730880460
Exac	rs730880460
Gnomad	rs730880460
Varsome	rs730880460
LitVar	rs730880460
Map	rs730880460
PheGenI	rs730880460
Biobank	rs730880460
1000 genomes	rs730880460
hgdp	rs730880460
ensembl	rs730880460
geneview	rs730880460
scholar	rs730880460
google	rs730880460
pharmgkb	rs730880460
gwascentral	rs730880460
openSNP	rs730880460
23andMe	rs730880460
SNPshot	rs730880460
SNPdbe	rs730880460
MSV3d	rs730880460
GWAS Ctlg	rs730880460

Max Magnitude

0

ClinVar
Risk	rs730880460(A;A) rs730880460(T;T)
Alt	rs730880460(A;A) rs730880460(T;T)
Reference	Rs730880460(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HRAS
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.533877C>A; NC_000011.9:g.533877C>T
CLNSRC
CLNACC	RCV000443979.1, RCV000157917.1,