rs397517042

Orientation

minus

Stabilized

minus

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

Make rs397517042(G;G)

Make rs397517042(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

25209896

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs397517042
dbSNP (classic)	rs397517042
ClinGen	rs397517042
ebi	rs397517042
HLI	rs397517042
Exac	rs397517042
Gnomad	rs397517042
Varsome	rs397517042
LitVar	rs397517042
Map	rs397517042
PheGenI	rs397517042
Biobank	rs397517042
1000 genomes	rs397517042
hgdp	rs397517042
ensembl	rs397517042
geneview	rs397517042
scholar	rs397517042
google	rs397517042
pharmgkb	rs397517042
gwascentral	rs397517042
openSNP	rs397517042
23andMe	rs397517042
SNPshot	rs397517042
SNPdbe	rs397517042
MSV3d	rs397517042
GWAS Ctlg	rs397517042

Max Magnitude

0

ClinVar
Risk	rs397517042(A;A) rs397517042(G;G)
Alt	rs397517042(A;A) rs397517042(G;G)
Reference	Rs397517042(T;T)
Significance	Pathogenic
Disease	Noonan syndrome not provided Rasopathy
Variation	info
Gene	KRAS
CLNDBN	Noonan syndrome not provided Rasopathy
Reversed	1
HGVS	NC_000012.11:g.25362830A>C; NC_000012.11:g.25362830A>T
CLNSRC
CLNACC	RCV000038275.3, RCV000157941.1, RCV000150884.1, RCV000493013.1,