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rs1057520688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520688(A;A)
Make rs1057520688(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133352516
GeneSURF1
is asnp
is mentioned by
dbSNPrs1057520688
dbSNP (old)rs1057520688
ClinGenrs1057520688
ebirs1057520688
HLIrs1057520688
Exacrs1057520688
Gnomadrs1057520688
Varsomers1057520688
Maprs1057520688
PheGenIrs1057520688
Biobankrs1057520688
1000 genomesrs1057520688
hgdprs1057520688
ensemblrs1057520688
gopubmedrs1057520688
geneviewrs1057520688
scholarrs1057520688
googlers1057520688
pharmgkbrs1057520688
gwascentralrs1057520688
openSNPrs1057520688
23andMers1057520688
23andMe allrs1057520688
SNPshotrs1057520688
SNPdbers1057520688
MSV3drs1057520688
GWAS Ctlgrs1057520688
Max Magnitude0
ClinVar
Risk rs1057520688(A;A)
Alt rs1057520688(A;A)
Reference Rs1057520688(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.136219371C>T
CLNSRC
CLNACC RCV000440906.1,