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

rs869312168

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312168(A;A)
Make rs869312168(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position73901424
GeneACTG2
is asnp
is mentioned by
dbSNPrs869312168
ebirs869312168
HLIrs869312168
Exacrs869312168
Varsomers869312168
Maprs869312168
PheGenIrs869312168
hapmaprs869312168
1000 genomesrs869312168
hgdprs869312168
ensemblrs869312168
gopubmedrs869312168
geneviewrs869312168
scholarrs869312168
googlers869312168
pharmgkbrs869312168
gwascentralrs869312168
openSNPrs869312168
23andMers869312168
23andMe allrs869312168
SNP Nexus

SNPshotrs869312168
SNPdbers869312168
MSV3drs869312168
GWAS Ctlgrs869312168
Max Magnitude0
ClinVar
Risk rs869312168(A;A)
Alt rs869312168(A;A)
Reference rs869312168(G;G)
Significance Pathogenic
Disease Chronic intestinal pseudoobstruction
Variation info
Gene ACTG2
CLNDBN Chronic intestinal pseudoobstruction
Reversed 0
HGVS NC_000002.11:g.74128551G>A
CLNSRC
CLNACC RCV000210357.1,