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rs375398247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs375398247(A;G)
Make rs375398247(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133353951
GeneSURF1
is asnp
is mentioned by
dbSNPrs375398247
dbSNP (classic)rs375398247
ClinGenrs375398247
ebirs375398247
HLIrs375398247
Exacrs375398247
Gnomadrs375398247
Varsomers375398247
LitVarrs375398247
Maprs375398247
PheGenIrs375398247
Biobankrs375398247
1000 genomesrs375398247
hgdprs375398247
ensemblrs375398247
geneviewrs375398247
scholarrs375398247
googlers375398247
pharmgkbrs375398247
gwascentralrs375398247
openSNPrs375398247
23andMers375398247
SNPshotrs375398247
SNPdbers375398247
MSV3drs375398247
GWAS Ctlgrs375398247
Max Magnitude0
ClinVar
Risk rs375398247(C;C) rs375398247(G;G)
Alt rs375398247(C;C) rs375398247(G;G)
Reference Rs375398247(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136220806A>C
CLNSRC
CLNACC RCV000198496.2,