Variant (rsID / SNP)

rs12976922

rs12976922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GARIN5B, FAM71E2. Location: chromosome 19, position 55,870,351. The table records no clinical significance for this variant.

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Reference-table entries

GARIN5BNot classified

Variant type: missense_variant
Chromosome / position: 19:55870351
HGVS: NM_001145402.2,c.1885A>G,p.Lys629Glu
Allele change: Missense_K629E

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.