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rs876657565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657565(C;T)
Make rs876657565(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position3396583
GenePRDM16
is asnp
is mentioned by
dbSNPrs876657565
dbSNP (classic)rs876657565
ClinGenrs876657565
ebirs876657565
HLIrs876657565
Exacrs876657565
Gnomadrs876657565
Varsomers876657565
LitVarrs876657565
Maprs876657565
PheGenIrs876657565
Biobankrs876657565
1000 genomesrs876657565
hgdprs876657565
ensemblrs876657565
geneviewrs876657565
scholarrs876657565
googlers876657565
pharmgkbrs876657565
gwascentralrs876657565
openSNPrs876657565
23andMers876657565
SNPshotrs876657565
SNPdbers876657565
MSV3drs876657565
GWAS Ctlgrs876657565
Max Magnitude0
ClinVar
Risk rs876657565(T;T)
Alt rs876657565(T;T)
Reference Rs876657565(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene PRDM16
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.3313147C>T
CLNSRC
CLNACC RCV000488452.1,