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rs606231408

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231408(C;G)
Make rs606231408(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position101774832
GeneFGF8
is asnp
is mentioned by
dbSNPrs606231408
ebirs606231408
HLIrs606231408
Exacrs606231408
Varsomers606231408
Maprs606231408
PheGenIrs606231408
hapmaprs606231408
1000 genomesrs606231408
hgdprs606231408
ensemblrs606231408
gopubmedrs606231408
geneviewrs606231408
scholarrs606231408
googlers606231408
pharmgkbrs606231408
gwascentralrs606231408
openSNPrs606231408
23andMers606231408
23andMe allrs606231408
SNP Nexus

SNPshotrs606231408
SNPdbers606231408
MSV3drs606231408
GWAS Ctlgrs606231408
Max Magnitude0
ClinVar
Risk rs606231408(G;G)
Alt rs606231408(G;G)
Reference rs606231408(C;C)
Significance Probable-Pathogenic
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103534589G>C
CLNSRC
CLNACC RCV000128829.1,