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rs377767435

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGA;CGA) 0 common in clinvar
(GAC;GAC) 0 common in clinvar
Make rs377767435(-;-)
Make rs377767435(-;GAC)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114491
GeneRET
is asnp
is mentioned by
dbSNPrs377767435
ebirs377767435
HLIrs377767435
Exacrs377767435
Varsomers377767435
Maprs377767435
PheGenIrs377767435
hapmaprs377767435
1000 genomesrs377767435
hgdprs377767435
ensemblrs377767435
gopubmedrs377767435
geneviewrs377767435
scholarrs377767435
googlers377767435
pharmgkbrs377767435
gwascentralrs377767435
openSNPrs377767435
23andMers377767435
23andMe allrs377767435
SNP Nexus

SNPshotrs377767435
SNPdbers377767435
MSV3drs377767435
GWAS Ctlgrs377767435
Max Magnitude0
ClinVar
Risk rs377767435(;)
Alt rs377767435(;)
Reference rs377767435(CGA;CGA)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43609939_43609941delGAC
CLNSRC ClinVar
CLNACC RCV000021810.1,