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rs397515419

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515419(C;T)
Make rs397515419(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position145917809
GeneGNRHR2, PEX11B
is asnp
is mentioned by
dbSNPrs397515419
ebirs397515419
HLIrs397515419
Exacrs397515419
Varsomers397515419
Maprs397515419
PheGenIrs397515419
hapmaprs397515419
1000 genomesrs397515419
hgdprs397515419
ensemblrs397515419
gopubmedrs397515419
geneviewrs397515419
scholarrs397515419
googlers397515419
pharmgkbrs397515419
gwascentralrs397515419
openSNPrs397515419
23andMers397515419
23andMe allrs397515419
SNP Nexus

SNPshotrs397515419
SNPdbers397515419
MSV3drs397515419
GWAS Ctlgrs397515419
Max Magnitude0
ClinVar
Risk rs397515419(T;T)
Alt rs397515419(T;T)
Reference rs397515419(C;C)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 14B
Variation info
Gene GNRHR2 PEX11B
CLNDBN Peroxisome biogenesis disorder 14B
Reversed 0
HGVS NC_000001.10:g.145517280C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032935.2,