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rs727505366

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505366(A;A)
Make rs727505366(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position57106004
GeneIL17RD
is asnp
is mentioned by
dbSNPrs727505366
ebirs727505366
HLIrs727505366
Exacrs727505366
Varsomers727505366
Maprs727505366
PheGenIrs727505366
hapmaprs727505366
1000 genomesrs727505366
hgdprs727505366
ensemblrs727505366
gopubmedrs727505366
geneviewrs727505366
scholarrs727505366
googlers727505366
pharmgkbrs727505366
gwascentralrs727505366
openSNPrs727505366
23andMers727505366
23andMe allrs727505366
SNP Nexus

SNPshotrs727505366
SNPdbers727505366
MSV3drs727505366
GWAS Ctlgrs727505366
Max Magnitude0
ClinVar
Risk rs727505366(A;A)
Alt rs727505366(A;A)
Reference rs727505366(G;G)
Significance Probable-Pathogenic
Disease Delayed puberty
Variation info
Gene IL17RD
CLNDBN Delayed puberty
Reversed 1
HGVS NC_000003.11:g.57140032C>T
CLNSRC
CLNACC RCV000156944.1,