Rs118204049

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204049(C;T)
Make rs118204049(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position67782840
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs118204049
PheGenIrs118204049
nextbiors118204049
hapmaprs118204049
1000 genomesrs118204049
hgdprs118204049
ensemblrs118204049
gopubmedrs118204049
geneviewrs118204049
scholarrs118204049
googlers118204049
pharmgkbrs118204049
gwascentralrs118204049
openSNPrs118204049
23andMers118204049
23andMe allrs118204049
SNP Nexus

SNPshotrs118204049
SNPdbers118204049
MSV3drs118204049
Max Magnitude0
OMIM612012
Desc
Variant0001
Relatedalso
ClinVar
Risk rs118204049(T;T)
Alt rs118204049(T;T)
Reference rs118204049(C;C)
Significance Pathogenic
Disease Spastic paraplegia 15
Variation info
Gene ZFYVE26
CLNDBN Spastic paraplegia 15
Reversed 1
HGVS NC_000014.8:g.68249557G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000785.1,