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rs672601361

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs672601361(G;G)
Make rs672601361(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position100989721
GeneC10orf2
is asnp
is mentioned by
dbSNPrs672601361
ebirs672601361
HLIrs672601361
Exacrs672601361
Varsomers672601361
Maprs672601361
PheGenIrs672601361
hapmaprs672601361
1000 genomesrs672601361
hgdprs672601361
ensemblrs672601361
gopubmedrs672601361
geneviewrs672601361
scholarrs672601361
googlers672601361
pharmgkbrs672601361
gwascentralrs672601361
openSNPrs672601361
23andMers672601361
23andMe allrs672601361
SNP Nexus

SNPshotrs672601361
SNPdbers672601361
MSV3drs672601361
GWAS Ctlgrs672601361
Max Magnitude0
ClinVar
Risk rs672601361(G;G)
Alt rs672601361(G;G)
Reference rs672601361(T;T)
Significance Pathogenic
Disease Perrault syndrome 5
Variation info
Gene C10orf2
CLNDBN Perrault syndrome 5
Reversed 0
HGVS NC_000010.10:g.102749478T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149472.4,