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rs869312931

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312931(C;C)
Make rs869312931(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position2543589
GeneBRAT1
is asnp
is mentioned by
dbSNPrs869312931
ebirs869312931
HLIrs869312931
Exacrs869312931
Varsomers869312931
Maprs869312931
PheGenIrs869312931
hapmaprs869312931
1000 genomesrs869312931
hgdprs869312931
ensemblrs869312931
gopubmedrs869312931
geneviewrs869312931
scholarrs869312931
googlers869312931
pharmgkbrs869312931
gwascentralrs869312931
openSNPrs869312931
23andMers869312931
23andMe allrs869312931
SNP Nexus

SNPshotrs869312931
SNPdbers869312931
MSV3drs869312931
GWAS Ctlgrs869312931
Max Magnitude0
ClinVar
Risk rs869312931(C;C)
Alt rs869312931(C;C)
Reference rs869312931(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene BRAT1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000007.13:g.2583223C>G
CLNSRC
CLNACC RCV000210559.1,