rs727504662

Orientation

minus

Stabilized

minus

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

Make rs727504662(A;T)

Make rs727504662(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

25227310

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs727504662
dbSNP (classic)	rs727504662
ClinGen	rs727504662
ebi	rs727504662
HLI	rs727504662
Exac	rs727504662
Gnomad	rs727504662
Varsome	rs727504662
LitVar	rs727504662
Map	rs727504662
PheGenI	rs727504662
Biobank	rs727504662
1000 genomes	rs727504662
hgdp	rs727504662
ensembl	rs727504662
geneview	rs727504662
scholar	rs727504662
google	rs727504662
pharmgkb	rs727504662
gwascentral	rs727504662
openSNP	rs727504662
23andMe	rs727504662
SNPshot	rs727504662
SNPdbe	rs727504662
MSV3d	rs727504662
GWAS Ctlg	rs727504662

Max Magnitude

0

ClinVar
Risk	rs727504662(T;T)
Alt	rs727504662(T;T)
Reference	Rs727504662(A;A)
Significance	Pathogenic
Disease	Noonan syndrome
Variation	info
Gene	KRAS
CLNDBN	Noonan syndrome
Reversed	1
HGVS	NC_000012.11:g.25380244T>A
CLNSRC
CLNACC	RCV000155926.2,