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rs863224227

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224227(G;T)
Make rs863224227(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133352609
GeneSURF1
is asnp
is mentioned by
dbSNPrs863224227
ebirs863224227
HLIrs863224227
Exacrs863224227
Varsomers863224227
Maprs863224227
PheGenIrs863224227
hapmaprs863224227
1000 genomesrs863224227
hgdprs863224227
ensemblrs863224227
gopubmedrs863224227
geneviewrs863224227
scholarrs863224227
googlers863224227
pharmgkbrs863224227
gwascentralrs863224227
openSNPrs863224227
23andMers863224227
23andMe allrs863224227
SNP Nexus

SNPshotrs863224227
SNPdbers863224227
MSV3drs863224227
GWAS Ctlgrs863224227
Max Magnitude0
ClinVar
Risk rs863224227(T;T)
Alt rs863224227(T;T)
Reference rs863224227(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.136219464C>A
CLNSRC
CLNACC RCV000200597.2,