rs786205570

Orientation

plus

Stabilized

plus

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

Make rs786205570(A;A)

Make rs786205570(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

78478063

Gene

FRAS1

is a	snp
is	mentioned by
dbSNP	rs786205570
dbSNP (classic)	rs786205570
ClinGen	rs786205570
ebi	rs786205570
HLI	rs786205570
Exac	rs786205570
Gnomad	rs786205570
Varsome	rs786205570
LitVar	rs786205570
Map	rs786205570
PheGenI	rs786205570
Biobank	rs786205570
1000 genomes	rs786205570
hgdp	rs786205570
ensembl	rs786205570
geneview	rs786205570
scholar	rs786205570
google	rs786205570
pharmgkb	rs786205570
gwascentral	rs786205570
openSNP	rs786205570
23andMe	rs786205570
SNPshot	rs786205570
SNPdbe	rs786205570
MSV3d	rs786205570
GWAS Ctlg	rs786205570

Max Magnitude

0

ClinVar
Risk	rs786205570(A;A)
Alt	rs786205570(A;A)
Reference	Rs786205570(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FRAS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.79399217T>A
CLNSRC
CLNACC	RCV000171378.1,