Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909644(G;T)
Make rs121909644(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38413795
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909644
ebirs121909644
HLIrs121909644
Exacrs121909644
Varsomers121909644
Maprs121909644
PheGenIrs121909644
hapmaprs121909644
1000 genomesrs121909644
hgdprs121909644
ensemblrs121909644
gopubmedrs121909644
geneviewrs121909644
scholarrs121909644
googlers121909644
pharmgkbrs121909644
gwascentralrs121909644
openSNPrs121909644
23andMers121909644
23andMe allrs121909644
SNP Nexus

SNPshotrs121909644
SNPdbers121909644
MSV3drs121909644
GWAS Ctlgrs121909644
Max Magnitude0
OMIM136350
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121909644(T;T)
Alt rs121909644(T;T)
Reference rs121909644(G;G)
Significance Other
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 1
HGVS NC_000008.10:g.38271313C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030939.3,