rs863225073

Orientation

plus

Stabilized

plus

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

Make rs863225073(G;T)

Make rs863225073(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

114325871

Gene

CHAMP1

is a	snp
is	mentioned by
dbSNP	rs863225073
dbSNP (classic)	rs863225073
ClinGen	rs863225073
ebi	rs863225073
HLI	rs863225073
Exac	rs863225073
Gnomad	rs863225073
Varsome	rs863225073
LitVar	rs863225073
Map	rs863225073
PheGenI	rs863225073
Biobank	rs863225073
1000 genomes	rs863225073
hgdp	rs863225073
ensembl	rs863225073
geneview	rs863225073
scholar	rs863225073
google	rs863225073
pharmgkb	rs863225073
gwascentral	rs863225073
openSNP	rs863225073
23andMe	rs863225073
SNPshot	rs863225073
SNPdbe	rs863225073
MSV3d	rs863225073
GWAS Ctlg	rs863225073

Max Magnitude

0

ClinVar
Risk	rs863225073(T;T)
Alt	rs863225073(T;T)
Reference	Rs863225073(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHAMP1
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.115091346G>T
CLNSRC
CLNACC	RCV000202219.1,