Rs104894179

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894179
PheGenIrs104894179
nextbiors104894179
hapmaprs104894179
1000 genomesrs104894179
hgdprs104894179
ensemblrs104894179
gopubmedrs104894179
geneviewrs104894179
scholarrs104894179
googlers104894179
pharmgkbrs104894179
gwascentralrs104894179
openSNPrs104894179
23andMers104894179
23andMe allrs104894179
SNP Nexus

SNPshotrs104894179
SNPdbers104894179
MSV3drs104894179
GenePHYH
Chromosome10
Orientationminus
Position13325713
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894179(A;C)
Make rs104894179(C;C)
OMIM602026
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894179(C;C)
Alt rs104894179(C;C)
Reference rs104894179(A;A)
Significance 5
Disease Refsum disease
ClinVar info
Gene PHYH
CLNDBN Refsum disease, adult, 1
Reversed 1
CLNHGVS NC_000010.10:g.13325713T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008022.2