rs201824235

Orientation

plus

Stabilized

plus

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

Make rs201824235(A;T)

Make rs201824235(T;T)

Reference

GRCh38 38.1/142

Chromosome

4

Position

42963153

Gene

GRXCR1

is a	snp
is	mentioned by
dbSNP	rs201824235
dbSNP (classic)	rs201824235
ClinGen	rs201824235
ebi	rs201824235
HLI	rs201824235
Exac	rs201824235
Gnomad	rs201824235
Varsome	rs201824235
LitVar	rs201824235
Map	rs201824235
PheGenI	rs201824235
Biobank	rs201824235
1000 genomes	rs201824235
hgdp	rs201824235
ensembl	rs201824235
geneview	rs201824235
scholar	rs201824235
google	rs201824235
pharmgkb	rs201824235
gwascentral	rs201824235
openSNP	rs201824235
23andMe	rs201824235
SNPshot	rs201824235
SNPdbe	rs201824235
MSV3d	rs201824235
GWAS Ctlg	rs201824235

Max Magnitude

0

ClinVar
Risk	rs201824235(T;T)
Alt	rs201824235(T;T)
Reference	Rs201824235(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	GRXCR1
CLNDBN	Deafness, autosomal recessive 25
Reversed	0
HGVS	NC_000004.11:g.42965170A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000217.2,