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rs387906423

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906423(-;-)
Make rs387906423(-;T)
Make rs387906423(T;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position8618
GenePYY
is asnp
is mentioned by
dbSNPrs387906423
ebirs387906423
HLIrs387906423
Exacrs387906423
Varsomers387906423
Maprs387906423
PheGenIrs387906423
hapmaprs387906423
1000 genomesrs387906423
hgdprs387906423
ensemblrs387906423
gopubmedrs387906423
geneviewrs387906423
scholarrs387906423
googlers387906423
pharmgkbrs387906423
gwascentralrs387906423
openSNPrs387906423
23andMers387906423
23andMe allrs387906423
SNP Nexus

SNPshotrs387906423
SNPdbers387906423
MSV3drs387906423
GWAS Ctlgrs387906423
Max Magnitude0
ClinVar
Risk rs387906423(T;T)
Alt rs387906423(T;T)
Reference rs387906423(;)
Significance Pathogenic
Disease Neuropathy ataxia retinitis pigmentosa syndrome
Variation info
Gene ATP6
CLNDBN Neuropathy ataxia retinitis pigmentosa syndrome
Reversed 0
HGVS NC_012920.1:m.8618dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010283.4,