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rs104894104

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs104894104(C;T)
Make rs104894104(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971019
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs104894104
ebirs104894104
HLIrs104894104
Exacrs104894104
Varsomers104894104
Maprs104894104
PheGenIrs104894104
hapmaprs104894104
1000 genomesrs104894104
hgdprs104894104
ensemblrs104894104
gopubmedrs104894104
geneviewrs104894104
scholarrs104894104
googlers104894104
pharmgkbrs104894104
gwascentralrs104894104
openSNPrs104894104
23andMers104894104
23andMe allrs104894104
SNP Nexus

SNPshotrs104894104
SNPdbers104894104
MSV3drs104894104
GWAS Ctlgrs104894104
Max Magnitude0
OMIM600160
Desc
Variant0017
Relatedalso
ClinVar
Risk rs104894104(T;T)
Alt rs104894104(T;T)
Reference rs104894104(C;C)
Significance Other
Disease Melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, 2, susceptibility to
Reversed 1
HGVS NC_000009.11:g.21971018G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010031.1,