rs587782971

Orientation

minus

Stabilized

minus

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

Make rs587782971(C;C)

Make rs587782971(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

12608895

Gene

RAF1

is a	snp
is	mentioned by
dbSNP	rs587782971
dbSNP (classic)	rs587782971
ClinGen	rs587782971
ebi	rs587782971
HLI	rs587782971
Exac	rs587782971
Gnomad	rs587782971
Varsome	rs587782971
LitVar	rs587782971
Map	rs587782971
PheGenI	rs587782971
Biobank	rs587782971
1000 genomes	rs587782971
hgdp	rs587782971
ensembl	rs587782971
geneview	rs587782971
scholar	rs587782971
google	rs587782971
pharmgkb	rs587782971
gwascentral	rs587782971
openSNP	rs587782971
23andMe	rs587782971
SNPshot	rs587782971
SNPdbe	rs587782971
MSV3d	rs587782971
GWAS Ctlg	rs587782971

Max Magnitude

0

ClinVar
Risk	rs587782971(C;C)
Alt	rs587782971(C;C)
Reference	Rs587782971(T;T)
Significance	Probable-Pathogenic
Disease	Noonan syndrome
Variation	info
Gene	RAF1
CLNDBN	Noonan syndrome
Reversed	1
HGVS	NC_000003.11:g.12650394A>G
CLNSRC
CLNACC	RCV000143943.1,