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Variant (rsID / SNP)

rs121909541

ANG

rs121909541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANG. Location: chromosome 14, position 21,161,931. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ANGConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
14:21161931
Cytoband
14q11.2
HGVS
NM_001097577.3(ANG):c.208A>G (p.Ile70Val)
Allele change
Missense_I70V

Associated conditions / phenotypes

Amyotrophic lateral sclerosis type 9

Public references

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