rs137853001

Orientation

minus

Stabilized

minus

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

Make rs137853001(C;T)

Make rs137853001(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

54664256

Gene

PCDH15

is a	snp
is	mentioned by
dbSNP	rs137853001
dbSNP (classic)	rs137853001
ClinGen	rs137853001
ebi	rs137853001
HLI	rs137853001
Exac	rs137853001
Gnomad	rs137853001
Varsome	rs137853001
LitVar	rs137853001
Map	rs137853001
PheGenI	rs137853001
Biobank	rs137853001
1000 genomes	rs137853001
hgdp	rs137853001
ensembl	rs137853001
geneview	rs137853001
scholar	rs137853001
google	rs137853001
pharmgkb	rs137853001
gwascentral	rs137853001
openSNP	rs137853001
23andMe	rs137853001
SNPshot	rs137853001
SNPdbe	rs137853001
MSV3d	rs137853001
GWAS Ctlg	rs137853001

Max Magnitude

0

OMIM	605514
Desc
Variant	0002
Related	also

ClinVar
Risk	rs137853001(T;T)
Alt	rs137853001(T;T)
Reference	Rs137853001(C;C)
Significance	Other
Disease	Usher syndrome
Variation	info
Gene	PCDH15
CLNDBN	Usher syndrome, type 1F
Reversed	1
HGVS	NC_000010.10:g.56424016G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005216.4,