Rs104894154

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894154
PheGenIrs104894154
nextbiors104894154
hapmaprs104894154
1000 genomesrs104894154
hgdprs104894154
ensemblrs104894154
gopubmedrs104894154
geneviewrs104894154
scholarrs104894154
googlers104894154
pharmgkbrs104894154
gwascentralrs104894154
openSNPrs104894154
23andMers104894154
23andMe allrs104894154
SNP Nexus

SNPshotrs104894154
SNPdbers104894154
MSV3drs104894154
GeneCYP17A1
Chromosome10
Orientationminus
Position104595073
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894154(A;A)
Make rs104894154(A;G)
OMIM609300
Desc
Variant0030
Relatedalso
ClinVar
Risk rs104894154(A;A)
Alt rs104894154(A;A)
Reference rs104894154(G;G)
Significance 5
Disease Complete combined 17-alpha-hydroxylase/17, Malignant melanoma
ClinVar info
Gene CYP17A1
CLNDBN Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency, Malignant melanoma
Reversed 1
CLNHGVS NC_000010.10:g.104595073C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001876.1, RCV000068782.2