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rs1060499663

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499663(-;-)
Make rs1060499663(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38416013
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1060499663
dbSNP (old)rs1060499663
ClinGenrs1060499663
ebirs1060499663
HLIrs1060499663
Exacrs1060499663
Gnomadrs1060499663
Varsomers1060499663
Maprs1060499663
PheGenIrs1060499663
Biobankrs1060499663
1000 genomesrs1060499663
hgdprs1060499663
ensemblrs1060499663
gopubmedrs1060499663
geneviewrs1060499663
scholarrs1060499663
googlers1060499663
pharmgkbrs1060499663
gwascentralrs1060499663
openSNPrs1060499663
23andMers1060499663
23andMe allrs1060499663
SNPshotrs1060499663
SNPdbers1060499663
MSV3drs1060499663
GWAS Ctlgrs1060499663
Max Magnitude0
ClinVar
Risk rs1060499663(-;-)
Alt rs1060499663(-;-)
Reference Rs1060499663(G;G)
Significance Pathogenic
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 1
HGVS NC_000008.10:g.38273531delC
CLNSRC
CLNACC RCV000449624.1,