Rs16980598

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is asnp
is mentioned by
dbSNPrs16980598
hapmaprs16980598
hgdprs16980598
ensemblrs16980598
gopubmedrs16980598
scholarrs16980598
googlers16980598
pharmgkbrs16980598
hgvbaseg2prs16980598
medrefsnprs16980598
23andMers16980598
SNP Nexus

Y Chromrs16980598
ChromosomeY
Orientationplus
Position19370916
ReferenceGRCh37 37.1/131
GenotypeEffect
rs16980598(A;A)Relevant to haplogroup DE
rs16980598(A;G)*?
rs16980598(G;G)*?


Genotypes Magnitude Summary
Rs16980598(A;A) Relevant to haplogroup DE
? (A;A) (A;G) (G;G) 28
[PMID 18385274] This snp distinguishes haplogroups
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