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rs797044959

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044959(A;A)
Make rs797044959(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73914836
GeneACTG2
is asnp
is mentioned by
dbSNPrs797044959
ebirs797044959
HLIrs797044959
Exacrs797044959
Varsomers797044959
Maprs797044959
PheGenIrs797044959
hapmaprs797044959
1000 genomesrs797044959
hgdprs797044959
ensemblrs797044959
gopubmedrs797044959
geneviewrs797044959
scholarrs797044959
googlers797044959
pharmgkbrs797044959
gwascentralrs797044959
openSNPrs797044959
23andMers797044959
23andMe allrs797044959
SNP Nexus

SNPshotrs797044959
SNPdbers797044959
MSV3drs797044959
GWAS Ctlgrs797044959
Max Magnitude0
ClinVar
Risk rs797044959(A;A)
Alt rs797044959(A;A)
Reference rs797044959(G;G)
Significance Pathogenic
Disease Inborn genetic diseases Chronic intestinal pseudoobstruction Megacystis
Variation info
Gene ACTG2
CLNDBN Inborn genetic diseases Chronic intestinal pseudoobstruction Megacystis
Reversed 0
HGVS NC_000002.11:g.74141963G>A
CLNSRC
CLNACC RCV000190820.1, RCV000210360.1,