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rs145632008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145632008(C;T)
Make rs145632008(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position3417922
GenePRDM16
is asnp
is mentioned by
dbSNPrs145632008
ebirs145632008
HLIrs145632008
Exacrs145632008
Varsomers145632008
Maprs145632008
PheGenIrs145632008
hapmaprs145632008
1000 genomesrs145632008
hgdprs145632008
ensemblrs145632008
gopubmedrs145632008
geneviewrs145632008
scholarrs145632008
googlers145632008
pharmgkbrs145632008
gwascentralrs145632008
openSNPrs145632008
23andMers145632008
23andMe allrs145632008
SNP Nexus

SNPshotrs145632008
SNPdbers145632008
MSV3drs145632008
GWAS Ctlgrs145632008
Max Magnitude0
ClinVar
Risk rs145632008(A,T;A,T)
Alt rs145632008(A,T;A,T)
Reference rs145632008(C;C)
Significance Untested
Disease not specified
Variation info
Gene PRDM16
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.3334486C>A
CLNSRC ClinVar
CLNACC RCV000219521.1,


[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.