rs201850090

Orientation

plus

Stabilized

plus

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

Make rs201850090(C;T)

Make rs201850090(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

143342009

Gene

CLCN1

is a	snp
is	mentioned by
dbSNP	rs201850090
dbSNP (classic)	rs201850090
ClinGen	rs201850090
ebi	rs201850090
HLI	rs201850090
Exac	rs201850090
Gnomad	rs201850090
Varsome	rs201850090
LitVar	rs201850090
Map	rs201850090
PheGenI	rs201850090
Biobank	rs201850090
1000 genomes	rs201850090
hgdp	rs201850090
ensembl	rs201850090
geneview	rs201850090
scholar	rs201850090
google	rs201850090
pharmgkb	rs201850090
gwascentral	rs201850090
openSNP	rs201850090
23andMe	rs201850090
SNPshot	rs201850090
SNPdbe	rs201850090
MSV3d	rs201850090
GWAS Ctlg	rs201850090

Max Magnitude

0

ClinVar
Risk	rs201850090(T;T)
Alt	rs201850090(T;T)
Reference	Rs201850090(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CLCN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.143039102C>T
CLNSRC
CLNACC	RCV000437007.1,