rs137853187

Orientation

plus

Stabilized

plus

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

Make rs137853187(A;A)

Make rs137853187(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

72106180

Gene	ANAPC15, LRTOMT

is a	snp
is	mentioned by
dbSNP	rs137853187
dbSNP (classic)	rs137853187
ClinGen	rs137853187
ebi	rs137853187
HLI	rs137853187
Exac	rs137853187
Gnomad	rs137853187
Varsome	rs137853187
LitVar	rs137853187
Map	rs137853187
PheGenI	rs137853187
Biobank	rs137853187
1000 genomes	rs137853187
hgdp	rs137853187
ensembl	rs137853187
geneview	rs137853187
scholar	rs137853187
google	rs137853187
pharmgkb	rs137853187
gwascentral	rs137853187
openSNP	rs137853187
23andMe	rs137853187
SNPshot	rs137853187
SNPdbe	rs137853187
MSV3d	rs137853187
GWAS Ctlg	rs137853187

Max Magnitude

0

OMIM	612414
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137853187(A;A)
Alt	rs137853187(A;A)
Reference	Rs137853187(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	ANAPC15 LRTOMT
CLNDBN	Deafness, autosomal recessive 63
Reversed	0
HGVS	NC_000011.9:g.71817226G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000575.2,