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rs200088377

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200088377(A;A)
Make rs200088377(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position57106133
GeneIL17RD
is asnp
is mentioned by
dbSNPrs200088377
ebirs200088377
HLIrs200088377
Exacrs200088377
Varsomers200088377
Maprs200088377
PheGenIrs200088377
hapmaprs200088377
1000 genomesrs200088377
hgdprs200088377
ensemblrs200088377
gopubmedrs200088377
geneviewrs200088377
scholarrs200088377
googlers200088377
pharmgkbrs200088377
gwascentralrs200088377
openSNPrs200088377
23andMers200088377
23andMe allrs200088377
SNP Nexus

SNPshotrs200088377
SNPdbers200088377
MSV3drs200088377
GWAS Ctlgrs200088377
Max Magnitude0
ClinVar
Risk rs200088377(A;A)
Alt rs200088377(A;A)
Reference rs200088377(G;G)
Significance Probable-Pathogenic
Disease Delayed puberty
Variation info
Gene IL17RD
CLNDBN Delayed puberty
Reversed 0
HGVS NC_000003.11:g.57140161G>A
CLNSRC
CLNACC RCV000156942.1,