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rs1057524676

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524676(A;A)
Make rs1057524676(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position101774782
GeneFGF8
is asnp
is mentioned by
dbSNPrs1057524676
dbSNP (old)rs1057524676
ClinGenrs1057524676
ebirs1057524676
HLIrs1057524676
Exacrs1057524676
Gnomadrs1057524676
Varsomers1057524676
LitVarrs1057524676
Maprs1057524676
PheGenIrs1057524676
Biobankrs1057524676
1000 genomesrs1057524676
hgdprs1057524676
ensemblrs1057524676
gopubmedrs1057524676
geneviewrs1057524676
scholarrs1057524676
googlers1057524676
pharmgkbrs1057524676
gwascentralrs1057524676
openSNPrs1057524676
23andMers1057524676
23andMe allrs1057524676
SNPshotrs1057524676
SNPdbers1057524676
MSV3drs1057524676
GWAS Ctlgrs1057524676
Max Magnitude0
ClinVar
Risk rs1057524676(A;A)
Alt rs1057524676(A;A)
Reference Rs1057524676(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGF8
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.103534539A>T
CLNSRC
CLNACC RCV000419587.1,