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rs515726223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs515726223(G;G)
Make rs515726223(G;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position38424655
GeneFGFR1
is asnp
is mentioned by
dbSNPrs515726223
ebirs515726223
HLIrs515726223
Exacrs515726223
Varsomers515726223
Maprs515726223
PheGenIrs515726223
hapmaprs515726223
1000 genomesrs515726223
hgdprs515726223
ensemblrs515726223
gopubmedrs515726223
geneviewrs515726223
scholarrs515726223
googlers515726223
pharmgkbrs515726223
gwascentralrs515726223
openSNPrs515726223
23andMers515726223
23andMe allrs515726223
SNP Nexus

SNPshotrs515726223
SNPdbers515726223
MSV3drs515726223
GWAS Ctlgrs515726223
Max Magnitude0
ClinVar
Risk rs515726223(G;G)
Alt rs515726223(G;G)
Reference rs515726223(T;T)
Significance Pathogenic
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 0
HGVS NC_000008.10:g.38282173T>G
CLNSRC ClinVar Pin India
CLNACC RCV000119058.1,