rs267606920

Orientation

minus

Stabilized

minus

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

Make rs267606920(A;A)

Make rs267606920(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

114713911

Gene

NRAS

is a	snp
is	mentioned by
dbSNP	rs267606920
dbSNP (classic)	rs267606920
ClinGen	rs267606920
ebi	rs267606920
HLI	rs267606920
Exac	rs267606920
Gnomad	rs267606920
Varsome	rs267606920
LitVar	rs267606920
Map	rs267606920
PheGenI	rs267606920
Biobank	rs267606920
1000 genomes	rs267606920
hgdp	rs267606920
ensembl	rs267606920
geneview	rs267606920
scholar	rs267606920
google	rs267606920
pharmgkb	rs267606920
gwascentral	rs267606920
openSNP	rs267606920
23andMe	rs267606920
SNPshot	rs267606920
SNPdbe	rs267606920
MSV3d	rs267606920
GWAS Ctlg	rs267606920

Max Magnitude

0

ClinVar
Risk	rs267606920(A;A)
Alt	rs267606920(A;A)
Reference	Rs267606920(G;G)
Significance	Pathogenic
Disease	Noonan syndrome 6 not provided Noonan syndrome 1
Variation	info
Gene	NRAS
CLNDBN	Noonan syndrome 6 not provided Noonan syndrome 1
Reversed	1
HGVS	NC_000001.10:g.115256532C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014917.25, RCV000158982.2, RCV000208552.1,