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rs876657413

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657413(C;T)
Make rs876657413(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position100154922
GeneERLIN1
is asnp
is mentioned by
dbSNPrs876657413
ebirs876657413
HLIrs876657413
Exacrs876657413
Varsomers876657413
Maprs876657413
PheGenIrs876657413
hapmaprs876657413
1000 genomesrs876657413
hgdprs876657413
ensemblrs876657413
gopubmedrs876657413
geneviewrs876657413
scholarrs876657413
googlers876657413
pharmgkbrs876657413
gwascentralrs876657413
openSNPrs876657413
23andMers876657413
23andMe allrs876657413
SNP Nexus

SNPshotrs876657413
SNPdbers876657413
MSV3drs876657413
GWAS Ctlgrs876657413
Max Magnitude0
ClinVar
Risk rs876657413(T;T)
Alt rs876657413(T;T)
Reference rs876657413(C;C)
Significance Pathogenic
Disease Spastic paraplegia 62
Variation info
Gene ERLIN1
CLNDBN Spastic paraplegia 62, autosomal recessive
Reversed 1
HGVS NC_000010.10:g.101914679G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211709.1,