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rs200229088

From SNPedia

Orientationplus
Stabilizedplus
Make rs200229088(-;-)
Make rs200229088(-;TG)
Make rs200229088(TG;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position44701716
is asnp
is mentioned by
dbSNPrs200229088
dbSNP (old)rs200229088
ClinGenrs200229088
ebirs200229088
HLIrs200229088
Exacrs200229088
Gnomadrs200229088
Varsomers200229088
Maprs200229088
PheGenIrs200229088
Biobankrs200229088
1000 genomesrs200229088
hgdprs200229088
ensemblrs200229088
gopubmedrs200229088
geneviewrs200229088
scholarrs200229088
googlers200229088
pharmgkbrs200229088
gwascentralrs200229088
openSNPrs200229088
23andMers200229088
23andMe allrs200229088
SNP Nexus

SNPshotrs200229088
SNPdbers200229088
MSV3drs200229088
GWAS Ctlgrs200229088
Max Magnitude

[PMID 27640304OA-icon.png] Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.