rs1057520629

Orientation

minus

Stabilized

minus

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

Make rs1057520629(C;G)

Make rs1057520629(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

85901099

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057520629
dbSNP (classic)	rs1057520629
ClinGen	rs1057520629
ebi	rs1057520629
HLI	rs1057520629
Exac	rs1057520629
Gnomad	rs1057520629
Varsome	rs1057520629
LitVar	rs1057520629
Map	rs1057520629
PheGenI	rs1057520629
Biobank	rs1057520629
1000 genomes	rs1057520629
hgdp	rs1057520629
ensembl	rs1057520629
geneview	rs1057520629
scholar	rs1057520629
google	rs1057520629
pharmgkb	rs1057520629
gwascentral	rs1057520629
openSNP	rs1057520629
23andMe	rs1057520629
SNPshot	rs1057520629
SNPdbe	rs1057520629
MSV3d	rs1057520629
GWAS Ctlg	rs1057520629

Max Magnitude

0

ClinVar
Risk	rs1057520629(G;G)
Alt	rs1057520629(G;G)
Reference	Rs1057520629(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85156104G>C
CLNSRC
CLNACC	RCV000431379.1,