Variant (rsID / SNP)

rs3735081

rs3735081 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GIMAP7. Location: chromosome 7, position 150,217,248. The table records no clinical significance for this variant.

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Reference-table entries

GIMAP7Not classified

Variant type: synonymous_variant
Chromosome / position: 7:150217248
HGVS: NM_153236.4,c.186A>G,p.Val62Val
Allele change: Synonymous_V62V

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.