rs398122809

Orientation

minus

Stabilized

minus

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

Make rs398122809(-;AGA)

Make rs398122809(AGA;AGA)

Reference

GRCh37.p10 37.5/138

Chromosome

11

Position

534212

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs398122809
dbSNP (classic)	rs398122809
ClinGen	rs398122809
ebi	rs398122809
HLI	rs398122809
Exac	rs398122809
Gnomad	rs398122809
Varsome	rs398122809
LitVar	rs398122809
Map	rs398122809
PheGenI	rs398122809
Biobank	rs398122809
1000 genomes	rs398122809
hgdp	rs398122809
ensembl	rs398122809
geneview	rs398122809
scholar	rs398122809
google	rs398122809
pharmgkb	rs398122809
gwascentral	rs398122809
openSNP	rs398122809
23andMe	rs398122809
SNPshot	rs398122809
SNPdbe	rs398122809
MSV3d	rs398122809
GWAS Ctlg	rs398122809

Max Magnitude

0

ClinVar
Risk	rs398122809(AGA;AGA)
Alt	rs398122809(AGA;AGA)
Reference	Rs398122809(-;-)
Significance	Pathogenic
Disease	Costello syndrome
Variation	info
Gene	HRAS
CLNDBN	Costello syndrome
Reversed	1
HGVS	NC_000011.9:g.534213_534215dupTCT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022798.24,