Know any genomes at Twitter support? Contact us if you can help get their attention.

Rs104894742

From SNPedia
Jump to: navigation, search

Orientationplus
is asnp
is mentioned by
dbSNPrs104894742
PheGenIrs104894742
nextbiors104894742
hapmaprs104894742
1000 genomesrs104894742
hgdprs104894742
ensemblrs104894742
gopubmedrs104894742
geneviewrs104894742
scholarrs104894742
googlers104894742
pharmgkbrs104894742
gwascentralrs104894742
openSNPrs104894742
23andMers104894742
23andMe allrs104894742
SNP Nexus

SNPshotrs104894742
SNPdbers104894742
MSV3drs104894742
GeneAR
ChromosomeX
Orientationplus
Position67545150
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894742(A;A)
Make rs104894742(A;G)
OMIM313700
Desc
Variant0038
Relatedalso
ClinVar
Risk rs104894742(A;A)
Alt rs104894742(A;A)
Reference rs104894742(G;G)
Significance 5
Disease Reifenstein syndrome
ClinVar info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
CLNHGVS NC_000023.10:g.66764992G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010515.1