rs397516825

Orientation

minus

Stabilized

minus

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

Make rs397516825(A;G)

Make rs397516825(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12604204

Gene

RAF1

is a	snp
is	mentioned by
dbSNP	rs397516825
dbSNP (classic)	rs397516825
ClinGen	rs397516825
ebi	rs397516825
HLI	rs397516825
Exac	rs397516825
Gnomad	rs397516825
Varsome	rs397516825
LitVar	rs397516825
Map	rs397516825
PheGenI	rs397516825
Biobank	rs397516825
1000 genomes	rs397516825
hgdp	rs397516825
ensembl	rs397516825
geneview	rs397516825
scholar	rs397516825
google	rs397516825
pharmgkb	rs397516825
gwascentral	rs397516825
openSNP	rs397516825
23andMe	rs397516825
SNPshot	rs397516825
SNPdbe	rs397516825
MSV3d	rs397516825
GWAS Ctlg	rs397516825

Max Magnitude

0

ClinVar
Risk	rs397516825(G;G)
Alt	rs397516825(G;G)
Reference	Rs397516825(A;A)
Significance	Probable-Pathogenic
Disease	Noonan syndrome
Variation	info
Gene	RAF1
CLNDBN	Noonan syndrome
Reversed	1
HGVS	NC_000003.11:g.12645703T>C
CLNSRC	ClinVar
CLNACC	RCV000037699.2,