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rs104893884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893884(C;T)
Make rs104893884(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position44305045
GeneFGF10
is asnp
is mentioned by
dbSNPrs104893884
ebirs104893884
HLIrs104893884
Exacrs104893884
Varsomers104893884
Maprs104893884
PheGenIrs104893884
hapmaprs104893884
1000 genomesrs104893884
hgdprs104893884
ensemblrs104893884
gopubmedrs104893884
geneviewrs104893884
scholarrs104893884
googlers104893884
pharmgkbrs104893884
gwascentralrs104893884
openSNPrs104893884
23andMers104893884
23andMe allrs104893884
SNP Nexus

SNPshotrs104893884
SNPdbers104893884
MSV3drs104893884
GWAS Ctlgrs104893884
GMAF0.0004591
Max Magnitude0
OMIM602115
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893884(G,T;G,T)
Alt rs104893884(G,T;G,T)
Reference rs104893884(C;C)
Significance Pathogenic
Disease Congenital absence of salivary gland
Variation info
Gene FGF10
CLNDBN Congenital absence of salivary gland
Reversed 1
HGVS NC_000005.9:g.44305147G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007964.4,