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rs863224230

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACC;ACC) 0 common in clinvar
Make rs863224230(ACC;CCT)
Make rs863224230(CCT;CCT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133353882
GeneSURF1
is asnp
is mentioned by
dbSNPrs863224230
dbSNP (old)rs863224230
ClinGenrs863224230
ebirs863224230
HLIrs863224230
Exacrs863224230
Gnomadrs863224230
Varsomers863224230
Maprs863224230
PheGenIrs863224230
Biobankrs863224230
1000 genomesrs863224230
hgdprs863224230
ensemblrs863224230
gopubmedrs863224230
geneviewrs863224230
scholarrs863224230
googlers863224230
pharmgkbrs863224230
gwascentralrs863224230
openSNPrs863224230
23andMers863224230
23andMe allrs863224230
SNP Nexus

SNPshotrs863224230
SNPdbers863224230
MSV3drs863224230
GWAS Ctlgrs863224230
Max Magnitude0
ClinVar
Risk rs863224230(CCT;CCT)
Alt rs863224230(CCT;CCT)
Reference Rs863224230(ACC;ACC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.136220737_136220739delGGTinsAGG
CLNSRC
CLNACC RCV000198114.1,