rs397516815

Orientation

minus

Stabilized

minus

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

Make rs397516815(A;G)

Make rs397516815(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12585760

Gene

RAF1

is a	snp
is	mentioned by
dbSNP	rs397516815
dbSNP (classic)	rs397516815
ClinGen	rs397516815
ebi	rs397516815
HLI	rs397516815
Exac	rs397516815
Gnomad	rs397516815
Varsome	rs397516815
LitVar	rs397516815
Map	rs397516815
PheGenI	rs397516815
Biobank	rs397516815
1000 genomes	rs397516815
hgdp	rs397516815
ensembl	rs397516815
geneview	rs397516815
scholar	rs397516815
google	rs397516815
pharmgkb	rs397516815
gwascentral	rs397516815
openSNP	rs397516815
23andMe	rs397516815
SNPshot	rs397516815
SNPdbe	rs397516815
MSV3d	rs397516815
GWAS Ctlg	rs397516815

Max Magnitude

0

ClinVar
Risk	rs397516815(G;G)
Alt	rs397516815(G;G)
Reference	Rs397516815(A;A)
Significance	Pathogenic
Disease	Noonan syndrome not provided
Variation	info
Gene	RAF1
CLNDBN	Noonan syndrome not provided
Reversed	1
HGVS	NC_000003.11:g.12627259T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000037675.3, RCV000434022.1,