rs1057521475

Orientation

minus

Stabilized

minus

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

Make rs1057521475(A;A)

Make rs1057521475(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

86047479

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057521475
dbSNP (classic)	rs1057521475
ClinGen	rs1057521475
ebi	rs1057521475
HLI	rs1057521475
Exac	rs1057521475
Gnomad	rs1057521475
Varsome	rs1057521475
LitVar	rs1057521475
Map	rs1057521475
PheGenI	rs1057521475
Biobank	rs1057521475
1000 genomes	rs1057521475
hgdp	rs1057521475
ensembl	rs1057521475
geneview	rs1057521475
scholar	rs1057521475
google	rs1057521475
pharmgkb	rs1057521475
gwascentral	rs1057521475
openSNP	rs1057521475
23andMe	rs1057521475
SNPshot	rs1057521475
SNPdbe	rs1057521475
MSV3d	rs1057521475
GWAS Ctlg	rs1057521475

Max Magnitude

0

ClinVar
Risk	rs1057521475(A;A)
Alt	rs1057521475(A;A)
Reference	Rs1057521475(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85302483C>T
CLNSRC
CLNACC	RCV000419936.1,