rs267606855

Orientation

plus

Stabilized

plus

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

Make rs267606855(C;T)

Make rs267606855(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

42893495

Gene

GRXCR1

is a	snp
is	mentioned by
dbSNP	rs267606855
dbSNP (classic)	rs267606855
ClinGen	rs267606855
ebi	rs267606855
HLI	rs267606855
Exac	rs267606855
Gnomad	rs267606855
Varsome	rs267606855
LitVar	rs267606855
Map	rs267606855
PheGenI	rs267606855
Biobank	rs267606855
1000 genomes	rs267606855
hgdp	rs267606855
ensembl	rs267606855
geneview	rs267606855
scholar	rs267606855
google	rs267606855
pharmgkb	rs267606855
gwascentral	rs267606855
openSNP	rs267606855
23andMe	rs267606855
SNPshot	rs267606855
SNPdbe	rs267606855
MSV3d	rs267606855
GWAS Ctlg	rs267606855

Max Magnitude

0

ClinVar
Risk	rs267606855(T;T)
Alt	rs267606855(T;T)
Reference	Rs267606855(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	GRXCR1
CLNDBN	Deafness, autosomal recessive 25
Reversed	0
HGVS	NC_000004.11:g.42895512C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000218.2,