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rs104893832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893832(A;A)
Make rs104893832(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position13854777
GeneWNT7A
is asnp
is mentioned by
dbSNPrs104893832
ebirs104893832
HLIrs104893832
Exacrs104893832
Varsomers104893832
Maprs104893832
PheGenIrs104893832
hapmaprs104893832
1000 genomesrs104893832
hgdprs104893832
ensemblrs104893832
gopubmedrs104893832
geneviewrs104893832
scholarrs104893832
googlers104893832
pharmgkbrs104893832
gwascentralrs104893832
openSNPrs104893832
23andMers104893832
23andMe allrs104893832
SNP Nexus

SNPshotrs104893832
SNPdbers104893832
MSV3drs104893832
GWAS Ctlgrs104893832
Max Magnitude0
OMIM601570
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893832(A;A)
Alt rs104893832(A;A)
Reference rs104893832(G;G)
Significance Pathogenic
Disease Fuhrmann syndrome
Variation info
Gene WNT7A
CLNDBN Fuhrmann syndrome
Reversed 1
HGVS NC_000003.11:g.13896274C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008527.2,