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rs11722554

From SNPedia

Orientationplus
Stabilizedplus
Make rs11722554(A;A)
Make rs11722554(A;G)
Make rs11722554(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome4
Position5015156
GeneCYTL1
is asnp
is mentioned by
dbSNPrs11722554
dbSNP (classic)rs11722554
ClinGenrs11722554
ebirs11722554
HLIrs11722554
Exacrs11722554
Gnomadrs11722554
Varsomers11722554
LitVarrs11722554
Maprs11722554
PheGenIrs11722554
Biobankrs11722554
1000 genomesrs11722554
hgdprs11722554
ensemblrs11722554
geneviewrs11722554
scholarrs11722554
googlers11722554
pharmgkbrs11722554
gwascentralrs11722554
openSNPrs11722554
23andMers11722554
23andMe allrs11722554
SNPshotrs11722554
SNPdbers11722554
MSV3drs11722554
GWAS Ctlgrs11722554
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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