Variant (rsID / SNP)

rs641320

rs641320 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAIM. Location: chromosome 3, position 138,347,957. The table records no clinical significance for this variant.

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Reference-table entries

FAIMNot classified

Variant type: missense_variant
Chromosome / position: 3:138347957
HGVS: NM_001033030.2,c.451G>A,p.Ala151Thr
Allele change: Missense_A117T

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.