Variant (rsID / SNP)

rs6971091

rs6971091 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GARIN1B, FAM71F1. Location: chromosome 7, position 128,363,287. The table records no clinical significance for this variant.

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Reference-table entries

GARIN1BNot classified

Variant type: missense_variant
Chromosome / position: 7:128363287
HGVS: NM_032599.4,c.724G>A,p.Glu242Lys
Allele change: 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.