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rs1736454

From SNPedia

Merged intors707687
Orientationplus
Make rs1736454(C;C)
Make rs1736454(C;T)
Make rs1736454(T;T)
ReferenceGRCh38.p7 38.3/149
ChromosomeY
Position56978021
is asnp
is mentioned by
dbSNPrs1736454
dbSNP (classic)rs1736454
ClinGenrs1736454
ebirs1736454
HLIrs1736454
Exacrs1736454
Gnomadrs1736454
Varsomers1736454
LitVarrs1736454
Maprs1736454
PheGenIrs1736454
Biobankrs1736454
1000 genomesrs1736454
hgdprs1736454
ensemblrs1736454
geneviewrs1736454
scholarrs1736454
googlers1736454
pharmgkbrs1736454
gwascentralrs1736454
openSNPrs1736454
23andMers1736454
23andMe allrs1736454
SNPshotrs1736454
SNPdbers1736454
MSV3drs1736454
GWAS Ctlgrs1736454
Y Chromrs1736454
StatusMerged into rs707687
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.