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rs398124654

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124654(A;G)
Make rs398124654(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position14326491
GeneFLRT3, MACROD2
is asnp
is mentioned by
dbSNPrs398124654
ebirs398124654
HLIrs398124654
Exacrs398124654
Varsomers398124654
Maprs398124654
PheGenIrs398124654
hapmaprs398124654
1000 genomesrs398124654
hgdprs398124654
ensemblrs398124654
gopubmedrs398124654
geneviewrs398124654
scholarrs398124654
googlers398124654
pharmgkbrs398124654
gwascentralrs398124654
openSNPrs398124654
23andMers398124654
23andMe allrs398124654
SNP Nexus

SNPshotrs398124654
SNPdbers398124654
MSV3drs398124654
GWAS Ctlgrs398124654
Max Magnitude0
ClinVar
Risk rs398124654(G;G)
Alt rs398124654(G;G)
Reference rs398124654(A;A)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 21 with or without anosmia
Variation info
Gene MACROD2 FLRT3
CLNDBN Hypogonadotropic hypogonadism 21 with or without anosmia
Reversed 1
HGVS NC_000020.10:g.14307137T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000043605.2,