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rs143862573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143862573(A;A)
Make rs143862573(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position43119750
GeneRET
is asnp
is mentioned by
dbSNPrs143862573
dbSNP (classic)rs143862573
ClinGenrs143862573
ebirs143862573
HLIrs143862573
Exacrs143862573
Gnomadrs143862573
Varsomers143862573
LitVarrs143862573
Maprs143862573
PheGenIrs143862573
Biobankrs143862573
1000 genomesrs143862573
hgdprs143862573
ensemblrs143862573
geneviewrs143862573
scholarrs143862573
googlers143862573
pharmgkbrs143862573
gwascentralrs143862573
openSNPrs143862573
23andMers143862573
23andMe allrs143862573
SNPshotrs143862573
SNPdbers143862573
MSV3drs143862573
GWAS Ctlgrs143862573
Max Magnitude0
ClinVar
Risk rs143862573(A;A) rs143862573(T;T)
Alt rs143862573(A;A) rs143862573(T;T)
Reference Rs143862573(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43615198G>A
CLNSRC
CLNACC RCV000413101.1,