Variant (rsID / SNP)

rs13343696

rs13343696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRRM5, ZNF428. Location: chromosome 19, position 44,116,956. The table records no clinical significance for this variant.

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Reference-table entries

SRRM5Not classified

Variant type: missense_variant
Chromosome / position: 19:44116956
HGVS: NM_001145641.2,c.683A>G,p.Lys228Arg
Allele change: Silent

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.