rs1057518086

Orientation

minus

Stabilized

minus

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

Make rs1057518086(C;C)

Make rs1057518086(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

81512312

Gene	ACTG1, FSCN2

is a	snp
is	mentioned by
dbSNP	rs1057518086
dbSNP (classic)	rs1057518086
ClinGen	rs1057518086
ebi	rs1057518086
HLI	rs1057518086
Exac	rs1057518086
Gnomad	rs1057518086
Varsome	rs1057518086
LitVar	rs1057518086
Map	rs1057518086
PheGenI	rs1057518086
Biobank	rs1057518086
1000 genomes	rs1057518086
hgdp	rs1057518086
ensembl	rs1057518086
geneview	rs1057518086
scholar	rs1057518086
google	rs1057518086
pharmgkb	rs1057518086
gwascentral	rs1057518086
openSNP	rs1057518086
23andMe	rs1057518086
SNPshot	rs1057518086
SNPdbe	rs1057518086
MSV3d	rs1057518086
GWAS Ctlg	rs1057518086

Max Magnitude

0

ClinVar
Risk	rs1057518086(C;C)
Alt	rs1057518086(C;C)
Reference	Rs1057518086(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FSCN2 ACTG1
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.79479338C>G
CLNSRC
CLNACC	RCV000413555.1,