rs1057519855

Orientation

minus

Stabilized

minus

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

Make rs1057519855(AG;GT)

Make rs1057519855(GT;GT)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

533873

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs1057519855
dbSNP (classic)	rs1057519855
ClinGen	rs1057519855
ebi	rs1057519855
HLI	rs1057519855
Exac	rs1057519855
Gnomad	rs1057519855
Varsome	rs1057519855
LitVar	rs1057519855
Map	rs1057519855
PheGenI	rs1057519855
Biobank	rs1057519855
1000 genomes	rs1057519855
hgdp	rs1057519855
ensembl	rs1057519855
geneview	rs1057519855
scholar	rs1057519855
google	rs1057519855
pharmgkb	rs1057519855
gwascentral	rs1057519855
openSNP	rs1057519855
23andMe	rs1057519855
SNPshot	rs1057519855
SNPdbe	rs1057519855
MSV3d	rs1057519855
GWAS Ctlg	rs1057519855

Max Magnitude

0

ClinVar
Risk	rs1057519855(GA;GA) rs1057519855(GT;GT)
Alt	rs1057519855(GA;GA) rs1057519855(GT;GT)
Reference	Rs1057519855(AG;AG)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	HRAS
CLNDBN	Neoplasm
Reversed	1
HGVS	NC_000011.9:g.533873_533874delCTinsAC; NC_000011.9:g.533873_533874delCTinsTC
CLNSRC
CLNACC	RCV000435225.1, RCV000418005.1,