Rs104893885

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893885(G;T)
Make rs104893885(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position44388366
GeneFGF10, FGF10-AS1
is asnp
is mentioned by
dbSNPrs104893885
PheGenIrs104893885
nextbiors104893885
hapmaprs104893885
1000 genomesrs104893885
hgdprs104893885
ensemblrs104893885
gopubmedrs104893885
geneviewrs104893885
scholarrs104893885
googlers104893885
pharmgkbrs104893885
gwascentralrs104893885
openSNPrs104893885
23andMers104893885
23andMe allrs104893885
SNP Nexus

SNPshotrs104893885
SNPdbers104893885
MSV3drs104893885
Max Magnitude0
OMIM602115
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893885(T;T)
Alt rs104893885(T;T)
Reference rs104893885(G;G)
Significance Pathogenic
Disease Ladd syndrome
Variation info
Gene FGF10
CLNDBN Ladd syndrome
Reversed 1
HGVS NC_000005.9:g.44388468C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007966.1,