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rs157935

From SNPedia

Orientationplus
Stabilizedplus
Make rs157935(G;G)
Make rs157935(G;T)
Make rs157935(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position130900794
GeneLINC-PINT
is asnp
is mentioned by
dbSNPrs157935
ebirs157935
HLIrs157935
Exacrs157935
Varsomers157935
Maprs157935
PheGenIrs157935
hapmaprs157935
1000 genomesrs157935
hgdprs157935
ensemblrs157935
gopubmedrs157935
geneviewrs157935
scholarrs157935
googlers157935
pharmgkbrs157935
gwascentralrs157935
openSNPrs157935
23andMers157935
23andMe allrs157935
SNP Nexus

SNPshotrs157935
SNPdbers157935
MSV3drs157935
GWAS Ctlgrs157935
GMAF0.3301
Max Magnitude
? (G;G) (G;T) (T;T) 28
23andMe blog rs157935 T 1.23 Basal Cell Carcinoma parental imprinting effect

[PMID 19578363OA-icon.png] New common variants affecting susceptibility to basal cell carcinoma

OMIM613063
Desc
Variant
Relatedalso
GWAS snp
PMID [PMID 24403052OA-icon.png]
Trait Basal cell carcinoma
Title Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
Risk Allele T
P-val 9E-11
Odds Ratio 1.23 [1.15-1.31]