rs267606932

Orientation

minus

Stabilized

minus

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

Make rs267606932(A;A)

Make rs267606932(A;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

54183451

Gene

PCDH15

is a	snp
is	mentioned by
dbSNP	rs267606932
dbSNP (classic)	rs267606932
ClinGen	rs267606932
ebi	rs267606932
HLI	rs267606932
Exac	rs267606932
Gnomad	rs267606932
Varsome	rs267606932
LitVar	rs267606932
Map	rs267606932
PheGenI	rs267606932
Biobank	rs267606932
1000 genomes	rs267606932
hgdp	rs267606932
ensembl	rs267606932
geneview	rs267606932
scholar	rs267606932
google	rs267606932
pharmgkb	rs267606932
gwascentral	rs267606932
openSNP	rs267606932
23andMe	rs267606932
SNPshot	rs267606932
SNPdbe	rs267606932
MSV3d	rs267606932
GWAS Ctlg	rs267606932

Max Magnitude

0

ClinVar
Risk	rs267606932(A;A)
Alt	rs267606932(A;A)
Reference	Rs267606932(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	PCDH15
CLNDBN	Deafness, autosomal recessive 23
Reversed	1
HGVS	NC_000010.10:g.55943211A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005225.2,