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rs781948238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781948238(A;A)
Make rs781948238(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133354823
GeneSURF1, SURF2
is asnp
is mentioned by
dbSNPrs781948238
dbSNP (classic)rs781948238
ClinGenrs781948238
ebirs781948238
HLIrs781948238
Exacrs781948238
Gnomadrs781948238
Varsomers781948238
LitVarrs781948238
Maprs781948238
PheGenIrs781948238
Biobankrs781948238
1000 genomesrs781948238
hgdprs781948238
ensemblrs781948238
geneviewrs781948238
scholarrs781948238
googlers781948238
pharmgkbrs781948238
gwascentralrs781948238
openSNPrs781948238
23andMers781948238
SNPshotrs781948238
SNPdbers781948238
MSV3drs781948238
GWAS Ctlgrs781948238
Max Magnitude0
ClinVar
Risk rs781948238(A;A)
Alt rs781948238(A;A)
Reference Rs781948238(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF2 SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136221678C>A
CLNSRC
CLNACC RCV000422985.1,