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rs373551988

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373551988(A;A)
Make rs373551988(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133353855
GeneSURF1
is asnp
is mentioned by
dbSNPrs373551988
ebirs373551988
HLIrs373551988
Exacrs373551988
Varsomers373551988
Maprs373551988
PheGenIrs373551988
hapmaprs373551988
1000 genomesrs373551988
hgdprs373551988
ensemblrs373551988
gopubmedrs373551988
geneviewrs373551988
scholarrs373551988
googlers373551988
pharmgkbrs373551988
gwascentralrs373551988
openSNPrs373551988
23andMers373551988
23andMe allrs373551988
SNP Nexus

SNPshotrs373551988
SNPdbers373551988
MSV3drs373551988
GWAS Ctlgrs373551988
Max Magnitude0
ClinVar
Risk rs373551988(A;A)
Alt rs373551988(A;A)
Reference rs373551988(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136220710G>A
CLNSRC
CLNACC RCV000200389.1,