rs587782972

Orientation

minus

Stabilized

minus

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

Make rs587782972(G;T)

Make rs587782972(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

12591729

Gene

RAF1

is a	snp
is	mentioned by
dbSNP	rs587782972
dbSNP (classic)	rs587782972
ClinGen	rs587782972
ebi	rs587782972
HLI	rs587782972
Exac	rs587782972
Gnomad	rs587782972
Varsome	rs587782972
LitVar	rs587782972
Map	rs587782972
PheGenI	rs587782972
Biobank	rs587782972
1000 genomes	rs587782972
hgdp	rs587782972
ensembl	rs587782972
geneview	rs587782972
scholar	rs587782972
google	rs587782972
pharmgkb	rs587782972
gwascentral	rs587782972
openSNP	rs587782972
23andMe	rs587782972
SNPshot	rs587782972
SNPdbe	rs587782972
MSV3d	rs587782972
GWAS Ctlg	rs587782972

Max Magnitude

0

ClinVar
Risk	rs587782972(T;T)
Alt	rs587782972(T;T)
Reference	Rs587782972(G;G)
Significance	Probable-Pathogenic
Disease	Noonan syndrome
Variation	info
Gene	RAF1
CLNDBN	Noonan syndrome
Reversed	1
HGVS	NC_000003.11:g.12633228C>A
CLNSRC
CLNACC	RCV000143944.1,