rs1057524703

Orientation

minus

Stabilized

minus

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

Make rs1057524703(A;C)

Make rs1057524703(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

81511353

Gene	ACTG1, FSCN2

is a	snp
is	mentioned by
dbSNP	rs1057524703
dbSNP (classic)	rs1057524703
ClinGen	rs1057524703
ebi	rs1057524703
HLI	rs1057524703
Exac	rs1057524703
Gnomad	rs1057524703
Varsome	rs1057524703
LitVar	rs1057524703
Map	rs1057524703
PheGenI	rs1057524703
Biobank	rs1057524703
1000 genomes	rs1057524703
hgdp	rs1057524703
ensembl	rs1057524703
geneview	rs1057524703
scholar	rs1057524703
google	rs1057524703
pharmgkb	rs1057524703
gwascentral	rs1057524703
openSNP	rs1057524703
23andMe	rs1057524703
SNPshot	rs1057524703
SNPdbe	rs1057524703
MSV3d	rs1057524703
GWAS Ctlg	rs1057524703

Max Magnitude

0

ClinVar
Risk	rs1057524703(C;C)
Alt	rs1057524703(C;C)
Reference	Rs1057524703(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ACTG1
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.79478379T>G
CLNSRC
CLNACC	RCV000444848.1,