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rs781934508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781934508(C;T)
Make rs781934508(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133352441
GeneSURF1
is asnp
is mentioned by
dbSNPrs781934508
dbSNP (classic)rs781934508
ClinGenrs781934508
ebirs781934508
HLIrs781934508
Exacrs781934508
Gnomadrs781934508
Varsomers781934508
LitVarrs781934508
Maprs781934508
PheGenIrs781934508
Biobankrs781934508
1000 genomesrs781934508
hgdprs781934508
ensemblrs781934508
geneviewrs781934508
scholarrs781934508
googlers781934508
pharmgkbrs781934508
gwascentralrs781934508
openSNPrs781934508
23andMers781934508
SNPshotrs781934508
SNPdbers781934508
MSV3drs781934508
GWAS Ctlgrs781934508
Max Magnitude0
ClinVar
Risk rs781934508(T;T)
Alt rs781934508(T;T)
Reference Rs781934508(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136219296C>T
CLNSRC
CLNACC RCV000413105.1,