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rs1057520188

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520188(-;-)
Make rs1057520188(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position3402940
GenePRDM16
is asnp
is mentioned by
dbSNPrs1057520188
dbSNP (classic)rs1057520188
ClinGenrs1057520188
ebirs1057520188
HLIrs1057520188
Exacrs1057520188
Gnomadrs1057520188
Varsomers1057520188
LitVarrs1057520188
Maprs1057520188
PheGenIrs1057520188
Biobankrs1057520188
1000 genomesrs1057520188
hgdprs1057520188
ensemblrs1057520188
geneviewrs1057520188
scholarrs1057520188
googlers1057520188
pharmgkbrs1057520188
gwascentralrs1057520188
openSNPrs1057520188
23andMers1057520188
23andMe allrs1057520188
SNPshotrs1057520188
SNPdbers1057520188
MSV3drs1057520188
GWAS Ctlgrs1057520188
Max Magnitude0
ClinVar
Risk rs1057520188(-;-)
Alt rs1057520188(-;-)
Reference Rs1057520188(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PRDM16
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.3319504delG
CLNSRC
CLNACC RCV000442803.1,