Variant (rsID / SNP)

rs344560

rs344560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF14. Location: chromosome 19, position 6,665,020. The table records no clinical significance for this variant.

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Reference-table entries

TNFSF14Not classified

Variant type: missense_variant
Chromosome / position: 19:6665020
HGVS: NM_001376887.1,c.640A>G,p.Lys214Glu
Allele change: Missense_K214E

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.