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rs7006527

From SNPedia

Orientationplus
Stabilizedplus
Make rs7006527(A;A)
Make rs7006527(A;C)
Make rs7006527(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position100012277
GeneRGS22
is asnp
is mentioned by
dbSNPrs7006527
dbSNP (classic)rs7006527
ClinGenrs7006527
ebirs7006527
HLIrs7006527
Exacrs7006527
Gnomadrs7006527
Varsomers7006527
LitVarrs7006527
Maprs7006527
PheGenIrs7006527
Biobankrs7006527
1000 genomesrs7006527
hgdprs7006527
ensemblrs7006527
geneviewrs7006527
scholarrs7006527
googlers7006527
pharmgkbrs7006527
gwascentralrs7006527
openSNPrs7006527
23andMers7006527
SNPshotrs7006527
SNPdbers7006527
MSV3drs7006527
GWAS Ctlgrs7006527
GMAF0.1653
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 24403052OA-icon.png] Germline Sequence Variants in TGM3 and RGS22 Confer Risk of Basal Cell Carcinoma