rs1057520765

Orientation

minus

Stabilized

minus

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

Make rs1057520765(G;T)

Make rs1057520765(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

85981793

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057520765
dbSNP (classic)	rs1057520765
ClinGen	rs1057520765
ebi	rs1057520765
HLI	rs1057520765
Exac	rs1057520765
Gnomad	rs1057520765
Varsome	rs1057520765
LitVar	rs1057520765
Map	rs1057520765
PheGenI	rs1057520765
Biobank	rs1057520765
1000 genomes	rs1057520765
hgdp	rs1057520765
ensembl	rs1057520765
geneview	rs1057520765
scholar	rs1057520765
google	rs1057520765
pharmgkb	rs1057520765
gwascentral	rs1057520765
openSNP	rs1057520765
23andMe	rs1057520765
SNPshot	rs1057520765
SNPdbe	rs1057520765
MSV3d	rs1057520765
GWAS Ctlg	rs1057520765

Max Magnitude

0

ClinVar
Risk	rs1057520765(T;T)
Alt	rs1057520765(T;T)
Reference	Rs1057520765(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85236797C>A
CLNSRC
CLNACC	RCV000435190.1,