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rs515726225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726225(A;A)
Make rs515726225(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position38414254
GeneFGFR1
is asnp
is mentioned by
dbSNPrs515726225
ebirs515726225
HLIrs515726225
Exacrs515726225
Varsomers515726225
Maprs515726225
PheGenIrs515726225
hapmaprs515726225
1000 genomesrs515726225
hgdprs515726225
ensemblrs515726225
gopubmedrs515726225
geneviewrs515726225
scholarrs515726225
googlers515726225
pharmgkbrs515726225
gwascentralrs515726225
openSNPrs515726225
23andMers515726225
23andMe allrs515726225
SNP Nexus

SNPshotrs515726225
SNPdbers515726225
MSV3drs515726225
GWAS Ctlgrs515726225
Max Magnitude0
ClinVar
Risk rs515726225(A;A)
Alt rs515726225(A;A)
Reference rs515726225(G;G)
Significance Pathogenic
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 0
HGVS NC_000008.10:g.38271772G>A
CLNSRC ClinVar Pin India
CLNACC RCV000119060.1,