Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1624844

FAM178B

rs1624844 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM178B. Location: chromosome 2, position 97,613,616. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

FAM178BNot classified
Variant type
synonymous_variant
Chromosome / position
2:97613616
HGVS
NM_001122646.3,c.1017A>G,p.Thr339Thr
Allele change
Synonymous_T339T

Public references

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