rs1057521251

Orientation

minus

Stabilized

minus

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

Make rs1057521251(G;T)

Make rs1057521251(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

153592547

Gene

FAM58A

is a	snp
is	mentioned by
dbSNP	rs1057521251
dbSNP (classic)	rs1057521251
ClinGen	rs1057521251
ebi	rs1057521251
HLI	rs1057521251
Exac	rs1057521251
Gnomad	rs1057521251
Varsome	rs1057521251
LitVar	rs1057521251
Map	rs1057521251
PheGenI	rs1057521251
Biobank	rs1057521251
1000 genomes	rs1057521251
hgdp	rs1057521251
ensembl	rs1057521251
geneview	rs1057521251
scholar	rs1057521251
google	rs1057521251
pharmgkb	rs1057521251
gwascentral	rs1057521251
openSNP	rs1057521251
23andMe	rs1057521251
SNPshot	rs1057521251
SNPdbe	rs1057521251
MSV3d	rs1057521251
GWAS Ctlg	rs1057521251

Max Magnitude

0

ClinVar
Risk	rs1057521251(T;T)
Alt	rs1057521251(T;T)
Reference	Rs1057521251(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FAM58A
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.152858005C>A
CLNSRC
CLNACC	RCV000434465.1,