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rs121909635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909635(A;A)
Make rs121909635(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position38426158
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909635
ebirs121909635
HLIrs121909635
Exacrs121909635
Varsomers121909635
Maprs121909635
PheGenIrs121909635
hapmaprs121909635
1000 genomesrs121909635
hgdprs121909635
ensemblrs121909635
gopubmedrs121909635
geneviewrs121909635
scholarrs121909635
googlers121909635
pharmgkbrs121909635
gwascentralrs121909635
openSNPrs121909635
23andMers121909635
23andMe allrs121909635
SNP Nexus

SNPshotrs121909635
SNPdbers121909635
MSV3drs121909635
GWAS Ctlgrs121909635
Max Magnitude0
OMIM136350
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121909635(A;A)
Alt rs121909635(A;A)
Reference rs121909635(G;G)
Significance Other
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 1
HGVS NC_000008.10:g.38283676C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017684.3,