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rs606231407

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231407(A;A)
Make rs606231407(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position101770613
GeneFGF8, LOC105378457
is asnp
is mentioned by
dbSNPrs606231407
ebirs606231407
HLIrs606231407
Exacrs606231407
Varsomers606231407
Maprs606231407
PheGenIrs606231407
hapmaprs606231407
1000 genomesrs606231407
hgdprs606231407
ensemblrs606231407
gopubmedrs606231407
geneviewrs606231407
scholarrs606231407
googlers606231407
pharmgkbrs606231407
gwascentralrs606231407
openSNPrs606231407
23andMers606231407
23andMe allrs606231407
SNP Nexus

SNPshotrs606231407
SNPdbers606231407
MSV3drs606231407
GWAS Ctlgrs606231407
Max Magnitude0
ClinVar
Risk rs606231407(A;A)
Alt rs606231407(A;A)
Reference rs606231407(G;G)
Significance Probable-Pathogenic
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103530370C>T
CLNSRC
CLNACC RCV000128828.1,