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rs200702528

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200702528(C;C)
Make rs200702528(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133352719
GeneSURF1
is asnp
is mentioned by
dbSNPrs200702528
ebirs200702528
HLIrs200702528
Exacrs200702528
Varsomers200702528
Maprs200702528
PheGenIrs200702528
hapmaprs200702528
1000 genomesrs200702528
hgdprs200702528
ensemblrs200702528
gopubmedrs200702528
geneviewrs200702528
scholarrs200702528
googlers200702528
pharmgkbrs200702528
gwascentralrs200702528
openSNPrs200702528
23andMers200702528
23andMe allrs200702528
SNP Nexus

SNPshotrs200702528
SNPdbers200702528
MSV3drs200702528
GWAS Ctlgrs200702528
Max Magnitude0
ClinVar
Risk rs200702528(C;C)
Alt rs200702528(C;C)
Reference rs200702528(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136219574T>C
CLNSRC
CLNACC RCV000196814.1,