rs397517041

Orientation

minus

Stabilized

minus

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

Make rs397517041(G;T)

Make rs397517041(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

25209908

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs397517041
dbSNP (classic)	rs397517041
ClinGen	rs397517041
ebi	rs397517041
HLI	rs397517041
Exac	rs397517041
Gnomad	rs397517041
Varsome	rs397517041
LitVar	rs397517041
Map	rs397517041
PheGenI	rs397517041
Biobank	rs397517041
1000 genomes	rs397517041
hgdp	rs397517041
ensembl	rs397517041
geneview	rs397517041
scholar	rs397517041
google	rs397517041
pharmgkb	rs397517041
gwascentral	rs397517041
openSNP	rs397517041
23andMe	rs397517041
SNPshot	rs397517041
SNPdbe	rs397517041
MSV3d	rs397517041
GWAS Ctlg	rs397517041

Max Magnitude

0

ClinVar
Risk	rs397517041(T;T)
Alt	rs397517041(T;T)
Reference	Rs397517041(G;G)
Significance	Probable-Pathogenic
Disease	Noonan syndrome
Variation	info
Gene	KRAS
CLNDBN	Noonan syndrome
Reversed	1
HGVS	NC_000012.11:g.25362842C>A
CLNSRC	ClinVar
CLNACC	RCV000038273.2,