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rs104893888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893888(A;C)
Make rs104893888(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position44388443
GeneFGF10, FGF10-AS1
is asnp
is mentioned by
dbSNPrs104893888
ebirs104893888
HLIrs104893888
Exacrs104893888
Varsomers104893888
Maprs104893888
PheGenIrs104893888
hapmaprs104893888
1000 genomesrs104893888
hgdprs104893888
ensemblrs104893888
gopubmedrs104893888
geneviewrs104893888
scholarrs104893888
googlers104893888
pharmgkbrs104893888
gwascentralrs104893888
openSNPrs104893888
23andMers104893888
23andMe allrs104893888
SNP Nexus

SNPshotrs104893888
SNPdbers104893888
MSV3drs104893888
GWAS Ctlgrs104893888
Max Magnitude0
OMIM602115
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104893888(C;C)
Alt rs104893888(C;C)
Reference rs104893888(A;A)
Significance Pathogenic
Disease Congenital absence of salivary gland
Variation info
Gene FGF10-AS1 LOC101927075 FGF10
CLNDBN Congenital absence of salivary gland
Reversed 1
HGVS NC_000005.9:g.44388545T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007970.3,