Rs104893889

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893889(A;A)
Make rs104893889(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position44310443
GeneFGF10
is asnp
is mentioned by
dbSNPrs104893889
Exacrs104893889
PheGenIrs104893889
nextbiors104893889
hapmaprs104893889
1000 genomesrs104893889
hgdprs104893889
ensemblrs104893889
gopubmedrs104893889
geneviewrs104893889
scholarrs104893889
googlers104893889
pharmgkbrs104893889
gwascentralrs104893889
openSNPrs104893889
23andMers104893889
23andMe allrs104893889
SNP Nexus

SNPshotrs104893889
SNPdbers104893889
MSV3drs104893889
OMIM602115
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104893889(A;A)
Alt rs104893889(A;A)
Reference rs104893889(G;G)
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.44310545C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007971.1,