Variant (rsID / SNP)

rs7669418

rs7669418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM131L. Location: chromosome 4, position 154,513,627. The table records no clinical significance for this variant.

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Reference-table entries

TMEM131LNot classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 4:154513627
HGVS: NM_001131007.2,c.1813A>G,p.Ile605Val
Allele change: Missense_I605V

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.