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rs41286560

From SNPedia

Orientationplus
Stabilizedplus
Make rs41286560(G;G)
Make rs41286560(G;T)
Make rs41286560(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position100883117
GeneMIR127, MIR136, MIR432, RTL1
is asnp
is mentioned by
dbSNPrs41286560
dbSNP (classic)rs41286560
ClinGenrs41286560
ebirs41286560
HLIrs41286560
Exacrs41286560
Gnomadrs41286560
Varsomers41286560
LitVarrs41286560
Maprs41286560
PheGenIrs41286560
Biobankrs41286560
1000 genomesrs41286560
hgdprs41286560
ensemblrs41286560
geneviewrs41286560
scholarrs41286560
googlers41286560
pharmgkbrs41286560
gwascentralrs41286560
openSNPrs41286560
23andMers41286560
SNPshotrs41286560
SNPdbers41286560
MSV3drs41286560
GWAS Ctlgrs41286560
Max Magnitude0

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