Variant (rsID / SNP)

rs17854363

rs17854363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM131B. Location: chromosome 7, position 143,053,723. The table records no clinical significance for this variant.

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Reference-table entries

FAM131BNot classified

Variant type: missense_variant
Chromosome / position: 7:143053723
HGVS: NM_001031690.3,c.1003G>A,p.Ala335Thr
Allele change: Missense_A307T

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.