rs767271426

Orientation

plus

Stabilized

plus

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

Make rs767271426(-;-)

Make rs767271426(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

16053708

Gene

CLCNKB

is a	snp
is	mentioned by
dbSNP	rs767271426
dbSNP (classic)	rs767271426
ClinGen	rs767271426
ebi	rs767271426
HLI	rs767271426
Exac	rs767271426
Gnomad	rs767271426
Varsome	rs767271426
LitVar	rs767271426
Map	rs767271426
PheGenI	rs767271426
Biobank	rs767271426
1000 genomes	rs767271426
hgdp	rs767271426
ensembl	rs767271426
geneview	rs767271426
scholar	rs767271426
google	rs767271426
pharmgkb	rs767271426
gwascentral	rs767271426
openSNP	rs767271426
23andMe	rs767271426
SNPshot	rs767271426
SNPdbe	rs767271426
MSV3d	rs767271426
GWAS Ctlg	rs767271426

Max Magnitude

0

ClinVar
Risk	rs767271426(-;-)
Alt	rs767271426(-;-)
Reference	Rs767271426(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLCNKB
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.16380203delG
CLNSRC
CLNACC	RCV000224201.1,