Rs104893886

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893886(G;G)
Make rs104893886(G;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position44305155
GeneFGF10
is asnp
is mentioned by
dbSNPrs104893886
PheGenIrs104893886
nextbiors104893886
hapmaprs104893886
1000 genomesrs104893886
hgdprs104893886
ensemblrs104893886
gopubmedrs104893886
geneviewrs104893886
scholarrs104893886
googlers104893886
pharmgkbrs104893886
gwascentralrs104893886
openSNPrs104893886
23andMers104893886
23andMe allrs104893886
SNP Nexus

SNPshotrs104893886
SNPdbers104893886
MSV3drs104893886
Max Magnitude0
OMIM602115
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893886(G;G)
Alt rs104893886(G;G)
Reference rs104893886(T;T)
Significance Pathogenic
Disease Ladd syndrome
Variation info
Gene FGF10
CLNDBN Ladd syndrome
Reversed 1
HGVS NC_000005.9:g.44305257A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007967.1,