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rs690016537

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs690016537(C;T)
Make rs690016537(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position70300842
GeneFAM136A
is asnp
is mentioned by
dbSNPrs690016537
ebirs690016537
HLIrs690016537
Exacrs690016537
Varsomers690016537
Maprs690016537
PheGenIrs690016537
hapmaprs690016537
1000 genomesrs690016537
hgdprs690016537
ensemblrs690016537
gopubmedrs690016537
geneviewrs690016537
scholarrs690016537
googlers690016537
pharmgkbrs690016537
gwascentralrs690016537
openSNPrs690016537
23andMers690016537
23andMe allrs690016537
SNP Nexus

SNPshotrs690016537
SNPdbers690016537
MSV3drs690016537
GWAS Ctlgrs690016537
Max Magnitude0
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,