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rs61730641

From SNPedia

Orientationplus
Stabilizedplus
Make rs61730641(C;C)
Make rs61730641(C;T)
Make rs61730641(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome4
Position86809827
GenePTPN13
is asnp
is mentioned by
dbSNPrs61730641
dbSNP (classic)rs61730641
ClinGenrs61730641
ebirs61730641
HLIrs61730641
Exacrs61730641
Gnomadrs61730641
Varsomers61730641
LitVarrs61730641
Maprs61730641
PheGenIrs61730641
Biobankrs61730641
1000 genomesrs61730641
hgdprs61730641
ensemblrs61730641
geneviewrs61730641
scholarrs61730641
googlers61730641
pharmgkbrs61730641
gwascentralrs61730641
openSNPrs61730641
23andMers61730641
23andMe allrs61730641
SNPshotrs61730641
SNPdbers61730641
MSV3drs61730641
GWAS Ctlgrs61730641
Max Magnitude0

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