Variant (rsID / SNP)

rs3795842

rs3795842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GARIN4, FAM71A. Location: chromosome 1, position 212,799,949. The table records no clinical significance for this variant.

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Reference-table entries

GARIN4Not classified

Variant type: missense_variant
Chromosome / position: 1:212799949
HGVS: NM_153606.4,c.1730C>T,p.Thr577Met
Allele change: Missense_T577M

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.