Variant (rsID / SNP)

rs140514685

rs140514685 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RASGRP2. Location: chromosome 11, position 64,497,613. Clinical significance in the table: Likely benign.

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Reference-table entries

RASGRP2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:64497613
Cytoband: 11q13.1
HGVS: NM_001098671.2(RASGRP2):c.1466C>G (p.Ser489Cys)
Allele change: Missense_S489C

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.