Variant (rsID / SNP)

rs31208

rs31208 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GARIN3, FAM71B. Location: chromosome 5, position 156,589,585. The table records no clinical significance for this variant.

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Reference-table entries

GARIN3Not classified

Variant type: missense_variant
Chromosome / position: 5:156589585
HGVS: NM_130899.3,c.1691T>C,p.Met564Thr
Allele change: Missense_M564T

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.