rs397515412

Orientation

minus

Stabilized

minus

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

Make rs397515412(C;C)

Make rs397515412(C;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

78105913

Gene

CIB2

is a	snp
is	mentioned by
dbSNP	rs397515412
dbSNP (classic)	rs397515412
ClinGen	rs397515412
ebi	rs397515412
HLI	rs397515412
Exac	rs397515412
Gnomad	rs397515412
Varsome	rs397515412
LitVar	rs397515412
Map	rs397515412
PheGenI	rs397515412
Biobank	rs397515412
1000 genomes	rs397515412
hgdp	rs397515412
ensembl	rs397515412
geneview	rs397515412
scholar	rs397515412
google	rs397515412
pharmgkb	rs397515412
gwascentral	rs397515412
openSNP	rs397515412
23andMe	rs397515412
SNPshot	rs397515412
SNPdbe	rs397515412
MSV3d	rs397515412
GWAS Ctlg	rs397515412

Max Magnitude

0

ClinVar
Risk	rs397515412(C;C)
Alt	rs397515412(C;C)
Reference	Rs397515412(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CIB2
CLNDBN	Deafness, autosomal recessive 48
Reversed	1
HGVS	NC_000015.9:g.78398255A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000032889.3,