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rs104893886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893886(G;G)
Make rs104893886(G;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position44305155
GeneFGF10
is asnp
is mentioned by
dbSNPrs104893886
dbSNP (classic)rs104893886
ClinGenrs104893886
ebirs104893886
HLIrs104893886
Exacrs104893886
Gnomadrs104893886
Varsomers104893886
LitVarrs104893886
Maprs104893886
PheGenIrs104893886
Biobankrs104893886
1000 genomesrs104893886
hgdprs104893886
ensemblrs104893886
geneviewrs104893886
scholarrs104893886
googlers104893886
pharmgkbrs104893886
gwascentralrs104893886
openSNPrs104893886
23andMers104893886
SNPshotrs104893886
SNPdbers104893886
MSV3drs104893886
GWAS Ctlgrs104893886
Max Magnitude0
OMIM602115
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893886(G;G)
Alt rs104893886(G;G)
Reference Rs104893886(T;T)
Significance Pathogenic
Disease Levy-Hollister syndrome
Variation info
Gene FGF10
CLNDBN Levy-Hollister syndrome
Reversed 1
HGVS NC_000005.9:g.44305257A>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000007967.2,