rs1057517716

Orientation

minus

Stabilized

minus

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

Make rs1057517716(C;T)

Make rs1057517716(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

85901091

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057517716
dbSNP (classic)	rs1057517716
ClinGen	rs1057517716
ebi	rs1057517716
HLI	rs1057517716
Exac	rs1057517716
Gnomad	rs1057517716
Varsome	rs1057517716
LitVar	rs1057517716
Map	rs1057517716
PheGenI	rs1057517716
Biobank	rs1057517716
1000 genomes	rs1057517716
hgdp	rs1057517716
ensembl	rs1057517716
geneview	rs1057517716
scholar	rs1057517716
google	rs1057517716
pharmgkb	rs1057517716
gwascentral	rs1057517716
openSNP	rs1057517716
23andMe	rs1057517716
SNPshot	rs1057517716
SNPdbe	rs1057517716
MSV3d	rs1057517716
GWAS Ctlg	rs1057517716

Max Magnitude

0

ClinVar
Risk	rs1057517716(T;T)
Alt	rs1057517716(T;T)
Reference	Rs1057517716(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85156096G>A
CLNSRC
CLNACC	RCV000414063.1,