rs864309654

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(ATT;ATT)	0	common in clinvar
(I;I)	0	common genotype

Make rs864309654(-;-)

Make rs864309654(-;ATT)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

88518858

Gene

KITLG

is a	snp
is	mentioned by
dbSNP	rs864309654
dbSNP (classic)	rs864309654
ClinGen	rs864309654
ebi	rs864309654
HLI	rs864309654
Exac	rs864309654
Gnomad	rs864309654
Varsome	rs864309654
LitVar	rs864309654
Map	rs864309654
PheGenI	rs864309654
Biobank	rs864309654
1000 genomes	rs864309654
hgdp	rs864309654
ensembl	rs864309654
geneview	rs864309654
scholar	rs864309654
google	rs864309654
pharmgkb	rs864309654
gwascentral	rs864309654
openSNP	rs864309654
23andMe	rs864309654
SNPshot	rs864309654
SNPdbe	rs864309654
MSV3d	rs864309654
GWAS Ctlg	rs864309654

Max Magnitude

0

ClinVar
Risk	rs864309654(-;-)
Alt	rs864309654(-;-)
Reference	Rs864309654(ATT;ATT)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	KITLG
CLNDBN	Deafness, autosomal dominant 69
Reversed	1
HGVS	NC_000012.11:g.88912635_88912637delAAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000203244.3,