Variant (rsID / SNP)

rs2708743

rs2708743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF765-ZNF761, ZNF761. Location: chromosome 19, position 53,958,126. The table records no clinical significance for this variant.

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Reference-table entries

ZNF765-ZNF761Not classified

Variant type: missense_variant
Chromosome / position: 19:53958126
HGVS: NM_001350496.2,c.365T>G,p.Ile122Ser
Allele change: Missense_I122S

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.