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Variant (rsID / SNP)

rs6715329

FAM178B

rs6715329 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM178B. Location: chromosome 2, position 97,637,905. The table records no clinical significance for this variant.

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Reference-table entries

FAM178BNot classified
Variant type
missense_variant
Chromosome / position
2:97637905
HGVS
NM_001122646.3,c.297A>G,p.Ile99Met
Allele change
Missense_I99M

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.