rs755322824

Orientation

plus

Stabilized

plus

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

Make rs755322824(C;C)

Make rs755322824(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

533790

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs755322824
dbSNP (classic)	rs755322824
ClinGen	rs755322824
ebi	rs755322824
HLI	rs755322824
Exac	rs755322824
Gnomad	rs755322824
Varsome	rs755322824
LitVar	rs755322824
Map	rs755322824
PheGenI	rs755322824
Biobank	rs755322824
1000 genomes	rs755322824
hgdp	rs755322824
ensembl	rs755322824
geneview	rs755322824
scholar	rs755322824
google	rs755322824
pharmgkb	rs755322824
gwascentral	rs755322824
openSNP	rs755322824
23andMe	rs755322824
SNPshot	rs755322824
SNPdbe	rs755322824
MSV3d	rs755322824
GWAS Ctlg	rs755322824

Max Magnitude

0

ClinVar
Risk	rs755322824(C;C)
Alt	rs755322824(C;C)
Reference	Rs755322824(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HRAS
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.533790G>C
CLNSRC
CLNACC	RCV000207497.1,