rs118192102

Orientation

plus

Stabilized

plus

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

Make rs118192102(A;G)

Make rs118192102(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

8296

is a	snp
is	mentioned by
dbSNP	rs118192102
dbSNP (classic)	rs118192102
ClinGen	rs118192102
ebi	rs118192102
HLI	rs118192102
Exac	rs118192102
Gnomad	rs118192102
Varsome	rs118192102
LitVar	rs118192102
Map	rs118192102
PheGenI	rs118192102
Biobank	rs118192102
1000 genomes	rs118192102
hgdp	rs118192102
ensembl	rs118192102
geneview	rs118192102
scholar	rs118192102
google	rs118192102
pharmgkb	rs118192102
gwascentral	rs118192102
openSNP	rs118192102
23andMe	rs118192102
SNPshot	rs118192102
SNPdbe	rs118192102
MSV3d	rs118192102
GWAS Ctlg	rs118192102

Max Magnitude

0

ClinVar
Risk	rs118192102(G;G)
Alt	rs118192102(G;G)
Reference	Rs118192102(A;A)
Significance	Pathogenic
Disease	Diabetes-deafness syndrome maternally transmitted
Variation	info
Gene
CLNDBN	Diabetes-deafness syndrome maternally transmitted
Reversed	0
HGVS	NC_012920.1:m.8296A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010201.4,