rs137853004

Orientation

minus

Stabilized

minus

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

Make rs137853004(C;G)

Make rs137853004(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

54090041

Gene

PCDH15

is a	snp
is	mentioned by
dbSNP	rs137853004
dbSNP (classic)	rs137853004
ClinGen	rs137853004
ebi	rs137853004
HLI	rs137853004
Exac	rs137853004
Gnomad	rs137853004
Varsome	rs137853004
LitVar	rs137853004
Map	rs137853004
PheGenI	rs137853004
Biobank	rs137853004
1000 genomes	rs137853004
hgdp	rs137853004
ensembl	rs137853004
geneview	rs137853004
scholar	rs137853004
google	rs137853004
pharmgkb	rs137853004
gwascentral	rs137853004
openSNP	rs137853004
23andMe	rs137853004
SNPshot	rs137853004
SNPdbe	rs137853004
MSV3d	rs137853004
GWAS Ctlg	rs137853004

Max Magnitude

0

OMIM	605514
Desc
Variant	0009
Related	also

ClinVar
Risk	rs137853004(G;G)
Alt	rs137853004(G;G)
Reference	Rs137853004(C;C)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	PCDH15
CLNDBN	Usher syndrome, type 1F
Reversed	1
HGVS	NC_000010.10:g.55849801G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005224.2,