rs369106578

Orientation

plus

Stabilized

plus

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

Make rs369106578(A;A)

Make rs369106578(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

533536

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs369106578
dbSNP (classic)	rs369106578
ClinGen	rs369106578
ebi	rs369106578
HLI	rs369106578
Exac	rs369106578
Gnomad	rs369106578
Varsome	rs369106578
LitVar	rs369106578
Map	rs369106578
PheGenI	rs369106578
Biobank	rs369106578
1000 genomes	rs369106578
hgdp	rs369106578
ensembl	rs369106578
geneview	rs369106578
scholar	rs369106578
google	rs369106578
pharmgkb	rs369106578
gwascentral	rs369106578
openSNP	rs369106578
23andMe	rs369106578
SNPshot	rs369106578
SNPdbe	rs369106578
MSV3d	rs369106578
GWAS Ctlg	rs369106578

Max Magnitude

0

ClinVar
Risk	rs369106578(A;A)
Alt	rs369106578(A;A)
Reference	Rs369106578(G;G)
Significance	Probable-Pathogenic
Disease	not provided Costello syndrome
Variation	info
Gene	HRAS
CLNDBN	not provided Costello syndrome
Reversed	0
HGVS	NC_000011.9:g.533536G>A
CLNSRC
CLNACC	RCV000157922.2, RCV000471505.1,