rs886041178

Orientation

minus

Stabilized

minus

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

Chromosome

X

Position

85958923

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs886041178
dbSNP (classic)	rs886041178
ClinGen	rs886041178
ebi	rs886041178
HLI	rs886041178
Exac	rs886041178
Gnomad	rs886041178
Varsome	rs886041178
LitVar	rs886041178
Map	rs886041178
PheGenI	rs886041178
Biobank	rs886041178
1000 genomes	rs886041178
hgdp	rs886041178
ensembl	rs886041178
geneview	rs886041178
scholar	rs886041178
google	rs886041178
pharmgkb	rs886041178
gwascentral	rs886041178
openSNP	rs886041178
23andMe	rs886041178
SNPshot	rs886041178
SNPdbe	rs886041178
MSV3d	rs886041178
GWAS Ctlg	rs886041178

Max Magnitude

0

ClinVar
Risk	rs886041178(A;A) rs886041178(T;T)
Alt	rs886041178(A;A) rs886041178(T;T)
Reference	Rs886041178(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85213928G>A
CLNSRC
CLNACC	RCV000265578.1,