Variant (rsID / SNP)

rs758037

rs758037 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SH3RF2. Location: chromosome 5, position 145,393,364. The table records no clinical significance for this variant.

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Reference-table entries

SH3RF2Not classified

Variant type: missense_variant
Chromosome / position: 5:145393364
HGVS: NM_152550.4,c.799C>T,p.Arg267Cys
Allele change: Missense_R267C

Associated conditions / phenotypes

Mycobacterium Tuberculosis 1

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.