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rs104894955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894955(C;T)
Make rs104894955(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position47449438
GeneZNF41
is asnp
is mentioned by
dbSNPrs104894955
ebirs104894955
HLIrs104894955
Exacrs104894955
Varsomers104894955
Maprs104894955
PheGenIrs104894955
hapmaprs104894955
1000 genomesrs104894955
hgdprs104894955
ensemblrs104894955
gopubmedrs104894955
geneviewrs104894955
scholarrs104894955
googlers104894955
pharmgkbrs104894955
gwascentralrs104894955
openSNPrs104894955
23andMers104894955
23andMe allrs104894955
SNP Nexus

SNPshotrs104894955
SNPdbers104894955
MSV3drs104894955
GWAS Ctlgrs104894955
Max Magnitude0
OMIM314995
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894955(T;T)
Alt rs104894955(T;T)
Reference rs104894955(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ZNF41
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.47308837G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000088660.2,