Rs104893885

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Orientationminus
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
GeneFGF10, FGF10-AS1
Chromosome5
Orientationminus
Position44388366
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893885(G;T)
Make rs104893885(T;T)
OMIM602115
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893885(T;T)
Alt rs104893885(T;T)
Reference rs104893885(G;G)
Significance 5
Disease Ladd syndrome
ClinVar info
Gene FGF10
CLNDBN Ladd syndrome
Reversed 1
CLNHGVS NC_000005.9:g.44388468C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007966.1