rs690016537

Orientation

minus

Stabilized

minus

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

Make rs690016537(C;T)

Make rs690016537(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

70300842

Gene

FAM136A

is a	snp
is	mentioned by
dbSNP	rs690016537
dbSNP (classic)	rs690016537
ClinGen	rs690016537
ebi	rs690016537
HLI	rs690016537
Exac	rs690016537
Gnomad	rs690016537
Varsome	rs690016537
LitVar	rs690016537
Map	rs690016537
PheGenI	rs690016537
Biobank	rs690016537
1000 genomes	rs690016537
hgdp	rs690016537
ensembl	rs690016537
geneview	rs690016537
scholar	rs690016537
google	rs690016537
pharmgkb	rs690016537
gwascentral	rs690016537
openSNP	rs690016537
23andMe	rs690016537
SNPshot	rs690016537
SNPdbe	rs690016537
MSV3d	rs690016537
GWAS Ctlg	rs690016537

Max Magnitude

0

ClinVar
Risk	rs690016537(T;T)
Alt	rs690016537(T;T)
Reference	Rs690016537(C;C)
Significance	Pathogenic
Disease	Ménière's disease
Variation	info
Gene	FAM136A
CLNDBN	Ménière's disease
Reversed	1
HGVS	NC_000002.11:g.70527974G>A
CLNSRC
CLNACC	RCV000149519.2,