rs1057517715

Orientation

minus

Stabilized

minus

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

Make rs1057517715(C;T)

Make rs1057517715(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

85911292

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057517715
dbSNP (classic)	rs1057517715
ClinGen	rs1057517715
ebi	rs1057517715
HLI	rs1057517715
Exac	rs1057517715
Gnomad	rs1057517715
Varsome	rs1057517715
LitVar	rs1057517715
Map	rs1057517715
PheGenI	rs1057517715
Biobank	rs1057517715
1000 genomes	rs1057517715
hgdp	rs1057517715
ensembl	rs1057517715
geneview	rs1057517715
scholar	rs1057517715
google	rs1057517715
pharmgkb	rs1057517715
gwascentral	rs1057517715
openSNP	rs1057517715
23andMe	rs1057517715
SNPshot	rs1057517715
SNPdbe	rs1057517715
MSV3d	rs1057517715
GWAS Ctlg	rs1057517715

Max Magnitude

0

ClinVar
Risk	rs1057517715(T;T)
Alt	rs1057517715(T;T)
Reference	Rs1057517715(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85166297G>A
CLNSRC
CLNACC	RCV000413451.1,