rs193929331

Orientation

minus

Stabilized

minus

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

Make rs193929331(A;G)

Make rs193929331(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

25245372

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs193929331
dbSNP (classic)	rs193929331
ClinGen	rs193929331
ebi	rs193929331
HLI	rs193929331
Exac	rs193929331
Gnomad	rs193929331
Varsome	rs193929331
LitVar	rs193929331
Map	rs193929331
PheGenI	rs193929331
Biobank	rs193929331
1000 genomes	rs193929331
hgdp	rs193929331
ensembl	rs193929331
geneview	rs193929331
scholar	rs193929331
google	rs193929331
pharmgkb	rs193929331
gwascentral	rs193929331
openSNP	rs193929331
23andMe	rs193929331
SNPshot	rs193929331
SNPdbe	rs193929331
MSV3d	rs193929331
GWAS Ctlg	rs193929331

Max Magnitude

0

ClinVar
Risk	rs193929331(G;G)
Alt	rs193929331(G;G)
Reference	Rs193929331(A;A)
Significance	Pathogenic
Disease	Noonan syndrome 3 Rasopathy not provided
Variation	info
Gene	KRAS
CLNDBN	Noonan syndrome 3 Rasopathy not provided
Reversed	1
HGVS	NC_000012.11:g.25398306T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013427.20, RCV000149836.1, RCV000364781.1,