rs397515411

Orientation

minus

Stabilized

minus

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

Make rs397515411(C;C)

Make rs397515411(C;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

78109309

Gene

CIB2

is a	snp
is	mentioned by
dbSNP	rs397515411
dbSNP (classic)	rs397515411
ClinGen	rs397515411
ebi	rs397515411
HLI	rs397515411
Exac	rs397515411
Gnomad	rs397515411
Varsome	rs397515411
LitVar	rs397515411
Map	rs397515411
PheGenI	rs397515411
Biobank	rs397515411
1000 genomes	rs397515411
hgdp	rs397515411
ensembl	rs397515411
geneview	rs397515411
scholar	rs397515411
google	rs397515411
pharmgkb	rs397515411
gwascentral	rs397515411
openSNP	rs397515411
23andMe	rs397515411
SNPshot	rs397515411
SNPdbe	rs397515411
MSV3d	rs397515411
GWAS Ctlg	rs397515411

Max Magnitude

0

ClinVar
Risk	rs397515411(C;C)
Alt	rs397515411(C;C)
Reference	Rs397515411(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CIB2
CLNDBN	Deafness, autosomal recessive 48
Reversed	1
HGVS	NC_000015.9:g.78401651A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000032887.3,