rs151340625

Orientation

plus

Stabilized

plus

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

Make rs151340625(A;A)

Make rs151340625(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

50088867

Gene

CLCN5

is a	snp
is	mentioned by
dbSNP	rs151340625
dbSNP (classic)	rs151340625
ClinGen	rs151340625
ebi	rs151340625
HLI	rs151340625
Exac	rs151340625
Gnomad	rs151340625
Varsome	rs151340625
LitVar	rs151340625
Map	rs151340625
PheGenI	rs151340625
Biobank	rs151340625
1000 genomes	rs151340625
hgdp	rs151340625
ensembl	rs151340625
geneview	rs151340625
scholar	rs151340625
google	rs151340625
pharmgkb	rs151340625
gwascentral	rs151340625
openSNP	rs151340625
23andMe	rs151340625
SNPshot	rs151340625
SNPdbe	rs151340625
MSV3d	rs151340625
GWAS Ctlg	rs151340625

Max Magnitude

0

ClinVar
Risk	rs151340625(A;A)
Alt	rs151340625(A;A)
Reference	Rs151340625(G;G)
Significance	Pathogenic
Disease	Nephrolithiasis
Variation	info
Gene	CLCN5
CLNDBN	Nephrolithiasis, X-linked recessive
Reversed	0
HGVS	NC_000023.10:g.49853524G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012569.14,