rs759761559

Orientation

plus

Stabilized

plus

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

Make rs759761559(C;T)

Make rs759761559(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

143331264

Gene

CLCN1

is a	snp
is	mentioned by
dbSNP	rs759761559
dbSNP (classic)	rs759761559
ClinGen	rs759761559
ebi	rs759761559
HLI	rs759761559
Exac	rs759761559
Gnomad	rs759761559
Varsome	rs759761559
LitVar	rs759761559
Map	rs759761559
PheGenI	rs759761559
Biobank	rs759761559
1000 genomes	rs759761559
hgdp	rs759761559
ensembl	rs759761559
geneview	rs759761559
scholar	rs759761559
google	rs759761559
pharmgkb	rs759761559
gwascentral	rs759761559
openSNP	rs759761559
23andMe	rs759761559
SNPshot	rs759761559
SNPdbe	rs759761559
MSV3d	rs759761559
GWAS Ctlg	rs759761559

Max Magnitude

0

ClinVar
Risk	rs759761559(T;T)
Alt	rs759761559(T;T)
Reference	Rs759761559(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CLCN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.143028357C>T
CLNSRC
CLNACC	RCV000488375.1,