Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894871

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894871(A;A)
Make rs104894871(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position43949914
GeneNDP
is asnp
is mentioned by
dbSNPrs104894871
ebirs104894871
HLIrs104894871
Exacrs104894871
Varsomers104894871
Maprs104894871
PheGenIrs104894871
hapmaprs104894871
1000 genomesrs104894871
hgdprs104894871
ensemblrs104894871
gopubmedrs104894871
geneviewrs104894871
scholarrs104894871
googlers104894871
pharmgkbrs104894871
gwascentralrs104894871
openSNPrs104894871
23andMers104894871
23andMe allrs104894871
SNP Nexus

SNPshotrs104894871
SNPdbers104894871
MSV3drs104894871
GWAS Ctlgrs104894871
Max Magnitude0
OMIM300658
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894871(A;A)
Alt rs104894871(A;A)
Reference rs104894871(G;G)
Significance Pathogenic
Disease Atrophia bulborum hereditaria
Variation info
Gene NDP
CLNDBN Atrophia bulborum hereditaria
Reversed 1
HGVS NC_000023.10:g.43809160C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011429.5,