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rs114970039

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs114970039(C;C)
Make rs114970039(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position198754304
GenePTPRC
is asnp
is mentioned by
dbSNPrs114970039
ebirs114970039
HLIrs114970039
Exacrs114970039
Varsomers114970039
Maprs114970039
PheGenIrs114970039
hapmaprs114970039
1000 genomesrs114970039
hgdprs114970039
ensemblrs114970039
gopubmedrs114970039
geneviewrs114970039
scholarrs114970039
googlers114970039
pharmgkbrs114970039
gwascentralrs114970039
openSNPrs114970039
23andMers114970039
23andMe allrs114970039
SNP Nexus

SNPshotrs114970039
SNPdbers114970039
MSV3drs114970039
GWAS Ctlgrs114970039
Max Magnitude0
ClinVar
Risk rs114970039(C;C)
Alt rs114970039(C;C)
Reference rs114970039(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTPRC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.198723433T>C
CLNSRC
CLNACC RCV000171165.1,