Variant (rsID / SNP)

rs62394179

rs62394179 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRAMD2B. Location: chromosome 5, position 125,802,027. The table records no clinical significance for this variant.

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Reference-table entries

GRAMD2BNot classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 5:125802027
HGVS: NM_001146321.3,c.226G>A,p.Glu76Lys
Allele change: Silent

Associated conditions / phenotypes

Silent

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.