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rs387906942

From SNPedia

Orientationplus
Stabilizedplus
Make rs387906942(C;C)
Make rs387906942(C;G)
Make rs387906942(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position74530433
GeneAUP1, HTRA2
is asnp
is mentioned by
dbSNPrs387906942
dbSNP (old)rs387906942
ClinGenrs387906942
ebirs387906942
HLIrs387906942
Exacrs387906942
Varsomers387906942
Maprs387906942
PheGenIrs387906942
Biobankrs387906942
1000 genomesrs387906942
hgdprs387906942
ensemblrs387906942
gopubmedrs387906942
geneviewrs387906942
scholarrs387906942
googlers387906942
pharmgkbrs387906942
gwascentralrs387906942
openSNPrs387906942
23andMers387906942
23andMe allrs387906942
SNP Nexus

SNPshotrs387906942
SNPdbers387906942
MSV3drs387906942
GWAS Ctlgrs387906942
Max Magnitude
ClinVar
Risk rs387906942(G;G)
Alt rs387906942(G;G)
Reference rs387906942(C;C)
Significance Other
Disease Parkinson disease 13
Variation info
Gene HTRA2 AUP1
CLNDBN Parkinson disease 13
Reversed 0
HGVS NC_000002.11:g.74757560C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023546.4,