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rs104893997

From SNPedia

Merged intors1800454
Orientationminus
Stabilizedminus
Make rs104893997(A;A)
Make rs104893997(A;G)
Make rs104893997(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32832635
GeneTAP2
is asnp
is mentioned by
dbSNPrs104893997
dbSNP (old)rs104893997
ClinGenrs104893997
ebirs104893997
HLIrs104893997
Exacrs104893997
Varsomers104893997
Maprs104893997
PheGenIrs104893997
Biobankrs104893997
1000 genomesrs104893997
hgdprs104893997
ensemblrs104893997
gopubmedrs104893997
geneviewrs104893997
scholarrs104893997
googlers104893997
pharmgkbrs104893997
gwascentralrs104893997
openSNPrs104893997
23andMers104893997
23andMe allrs104893997
SNP Nexus

SNPshotrs104893997
SNPdbers104893997
MSV3drs104893997
GWAS Ctlgrs104893997
StatusMerged into rs1800454
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM170261
Desc
Variant0001
Relatedalso