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rs121909629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909629(A;A)
Make rs121909629(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position38415905
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909629
ebirs121909629
HLIrs121909629
Exacrs121909629
Varsomers121909629
Maprs121909629
PheGenIrs121909629
hapmaprs121909629
1000 genomesrs121909629
hgdprs121909629
ensemblrs121909629
gopubmedrs121909629
geneviewrs121909629
scholarrs121909629
googlers121909629
pharmgkbrs121909629
gwascentralrs121909629
openSNPrs121909629
23andMers121909629
23andMe allrs121909629
SNP Nexus

SNPshotrs121909629
SNPdbers121909629
MSV3drs121909629
GWAS Ctlgrs121909629
Max Magnitude0
OMIM136350
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909629(A;A)
Alt rs121909629(A;A)
Reference rs121909629(G;G)
Significance Other
Disease HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
Variation info
Gene FGFR1
CLNDBN HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO
Reversed 1
HGVS NC_000008.10:g.38273423C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030927.3,