rs55868108

Orientation

plus

Stabilized

plus

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

Make rs55868108(C;T)

Make rs55868108(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

232526603

Gene

CHRND

is a	snp
is	mentioned by
dbSNP	rs55868108
dbSNP (classic)	rs55868108
ClinGen	rs55868108
ebi	rs55868108
HLI	rs55868108
Exac	rs55868108
Gnomad	rs55868108
Varsome	rs55868108
LitVar	rs55868108
Map	rs55868108
PheGenI	rs55868108
Biobank	rs55868108
1000 genomes	rs55868108
hgdp	rs55868108
ensembl	rs55868108
geneview	rs55868108
scholar	rs55868108
google	rs55868108
pharmgkb	rs55868108
gwascentral	rs55868108
openSNP	rs55868108
23andMe	rs55868108
SNPshot	rs55868108
SNPdbe	rs55868108
MSV3d	rs55868108
GWAS Ctlg	rs55868108

Max Magnitude

0

ClinVar
Risk	rs55868108(T;T)
Alt	rs55868108(T;T)
Reference	Rs55868108(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHRND
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.233391313C>T
CLNSRC
CLNACC	RCV000485087.1,