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rs796052008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs796052008(GG;TA)
Make rs796052008(TA;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49444684
GeneMUT
is asnp
is mentioned by
dbSNPrs796052008
ClinGenrs796052008
ebirs796052008
HLIrs796052008
Exacrs796052008
Varsomers796052008
Maprs796052008
PheGenIrs796052008
hapmaprs796052008
1000 genomesrs796052008
hgdprs796052008
ensemblrs796052008
gopubmedrs796052008
geneviewrs796052008
scholarrs796052008
googlers796052008
pharmgkbrs796052008
gwascentralrs796052008
openSNPrs796052008
23andMers796052008
23andMe allrs796052008
SNP Nexus

SNPshotrs796052008
SNPdbers796052008
MSV3drs796052008
GWAS Ctlgrs796052008
Max Magnitude0
ClinVar
Risk rs796052008(TA;TA)
Alt rs796052008(TA;TA)
Reference Rs796052008(GG;GG)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49412397_49412398delCCinsTA
CLNSRC
CLNACC RCV000186061.2,