rs1057517714

Orientation

minus

Stabilized

minus

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

Make rs1057517714(A;A)

Make rs1057517714(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

85956300

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057517714
dbSNP (classic)	rs1057517714
ClinGen	rs1057517714
ebi	rs1057517714
HLI	rs1057517714
Exac	rs1057517714
Gnomad	rs1057517714
Varsome	rs1057517714
LitVar	rs1057517714
Map	rs1057517714
PheGenI	rs1057517714
Biobank	rs1057517714
1000 genomes	rs1057517714
hgdp	rs1057517714
ensembl	rs1057517714
geneview	rs1057517714
scholar	rs1057517714
google	rs1057517714
pharmgkb	rs1057517714
gwascentral	rs1057517714
openSNP	rs1057517714
23andMe	rs1057517714
SNPshot	rs1057517714
SNPdbe	rs1057517714
MSV3d	rs1057517714
GWAS Ctlg	rs1057517714

Max Magnitude

0

ClinVar
Risk	rs1057517714(A;A)
Alt	rs1057517714(A;A)
Reference	Rs1057517714(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85211305G>T
CLNSRC
CLNACC	RCV000414588.1,