rs786205604

Orientation

minus

Stabilized

minus

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

Make rs786205604(G;T)

Make rs786205604(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

85956175

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs786205604
dbSNP (classic)	rs786205604
ClinGen	rs786205604
ebi	rs786205604
HLI	rs786205604
Exac	rs786205604
Gnomad	rs786205604
Varsome	rs786205604
LitVar	rs786205604
Map	rs786205604
PheGenI	rs786205604
Biobank	rs786205604
1000 genomes	rs786205604
hgdp	rs786205604
ensembl	rs786205604
geneview	rs786205604
scholar	rs786205604
google	rs786205604
pharmgkb	rs786205604
gwascentral	rs786205604
openSNP	rs786205604
23andMe	rs786205604
SNPshot	rs786205604
SNPdbe	rs786205604
MSV3d	rs786205604
GWAS Ctlg	rs786205604

Max Magnitude

0

ClinVar
Risk	rs786205604(T;T)
Alt	rs786205604(T;T)
Reference	Rs786205604(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85211180C>A
CLNSRC
CLNACC	RCV000171441.1,