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rs377767397

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767397(A;A)
Make rs377767397(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43113628
GeneRET
is asnp
is mentioned by
dbSNPrs377767397
ebirs377767397
HLIrs377767397
Exacrs377767397
Varsomers377767397
Maprs377767397
PheGenIrs377767397
hapmaprs377767397
1000 genomesrs377767397
hgdprs377767397
ensemblrs377767397
gopubmedrs377767397
geneviewrs377767397
scholarrs377767397
googlers377767397
pharmgkbrs377767397
gwascentralrs377767397
openSNPrs377767397
23andMers377767397
23andMe allrs377767397
SNP Nexus

SNPshotrs377767397
SNPdbers377767397
MSV3drs377767397
GWAS Ctlgrs377767397
Max Magnitude0
ClinVar
Risk rs377767397(A,C,T;A,C,T)
Alt rs377767397(A,C,T;A,C,T)
Reference rs377767397(G;G)
Significance Pathogenic
Disease MEN2A and FMTC MEN2 phenotype: Unknown
Variation info
Gene RET
CLNDBN MEN2A and FMTC MEN2 phenotype: Unknown
Reversed 0
HGVS NC_000010.10:g.43609076G>A; NC_000010.10:g.43609076G>C; NC_000010.10:g.43609076G>T
CLNSRC ClinVar
CLNACC RCV000021784.1, RCV000021786.1, RCV000021787.1,