rs886041756

Orientation

minus

Stabilized

minus

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

Chromosome

17

Position

81511048

Gene	ACTG1, FSCN2

is a	snp
is	mentioned by
dbSNP	rs886041756
dbSNP (classic)	rs886041756
ClinGen	rs886041756
ebi	rs886041756
HLI	rs886041756
Exac	rs886041756
Gnomad	rs886041756
Varsome	rs886041756
LitVar	rs886041756
Map	rs886041756
PheGenI	rs886041756
Biobank	rs886041756
1000 genomes	rs886041756
hgdp	rs886041756
ensembl	rs886041756
geneview	rs886041756
scholar	rs886041756
google	rs886041756
pharmgkb	rs886041756
gwascentral	rs886041756
openSNP	rs886041756
23andMe	rs886041756
SNPshot	rs886041756
SNPdbe	rs886041756
MSV3d	rs886041756
GWAS Ctlg	rs886041756

Max Magnitude

0

ClinVar
Risk	rs886041756(G;G)
Alt	rs886041756(G;G)
Reference	Rs886041756(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ACTG1
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.79478074T>C
CLNSRC
CLNACC	RCV000293975.1,