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rs796052009

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052009(-;-)
Make rs796052009(-;GGA)
Make rs796052009(GGA;GGA)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49459092
GeneMUT
is asnp
is mentioned by
dbSNPrs796052009
ebirs796052009
HLIrs796052009
Exacrs796052009
Varsomers796052009
Maprs796052009
PheGenIrs796052009
hapmaprs796052009
1000 genomesrs796052009
hgdprs796052009
ensemblrs796052009
gopubmedrs796052009
geneviewrs796052009
scholarrs796052009
googlers796052009
pharmgkbrs796052009
gwascentralrs796052009
openSNPrs796052009
23andMers796052009
23andMe allrs796052009
SNP Nexus

SNPshotrs796052009
SNPdbers796052009
MSV3drs796052009
GWAS Ctlgrs796052009
Max Magnitude0
ClinVar
Risk rs796052009(GGA;GGA)
Alt rs796052009(GGA;GGA)
Reference rs796052009(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49426806_49426808dupTCC
CLNSRC
CLNACC RCV000186062.1,