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rs1078305

From SNPedia

Orientationminus
Make rs1078305(C;C)
Make rs1078305(C;T)
Make rs1078305(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position121289122
GeneGSN
is asnp
is mentioned by
dbSNPrs1078305
ebirs1078305
HLIrs1078305
Exacrs1078305
Varsomers1078305
Maprs1078305
PheGenIrs1078305
hapmaprs1078305
1000 genomesrs1078305
hgdprs1078305
ensemblrs1078305
gopubmedrs1078305
geneviewrs1078305
scholarrs1078305
googlers1078305
pharmgkbrs1078305
gwascentralrs1078305
openSNPrs1078305
23andMers1078305
23andMe allrs1078305
SNP Nexus

SNPshotrs1078305
SNPdbers1078305
MSV3drs1078305
GWAS Ctlgrs1078305
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26848502] Gelsolin rs1078305 and rs10818524 polymorphisms were associated with risk of oral squamous cell carcinoma in a Chinese Han population.