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

rs796052941

From SNPedia

Orientationplus
Make rs796052941(-;-)
Make rs796052941(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position29814424
GenePAGR1, PRRT2
is asnp
is mentioned by
dbSNPrs796052941
ClinGenrs796052941
ebirs796052941
HLIrs796052941
Exacrs796052941
Varsomers796052941
Maprs796052941
PheGenIrs796052941
hapmaprs796052941
1000 genomesrs796052941
hgdprs796052941
ensemblrs796052941
gopubmedrs796052941
geneviewrs796052941
scholarrs796052941
googlers796052941
pharmgkbrs796052941
gwascentralrs796052941
openSNPrs796052941
23andMers796052941
23andMe allrs796052941
SNP Nexus

SNPshotrs796052941
SNPdbers796052941
MSV3drs796052941
GWAS Ctlgrs796052941
Max Magnitude
ClinVar
Risk
Alt
Reference Rs796052941(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAGR1 PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29825745delG
CLNSRC
CLNACC RCV000188780.2,