SNP Report
Name | rs834811 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:136199823 - 136199823(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.480831 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000445293, ENST00000435996); non_coding_transcript_variant(ENST00000445293, ENST00000435996) | ||
SIFT Annotation | deleterious_-_low_confidence; tolerated | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000435723); tolerated(ENST00000393085) | ||
PolyPhen Annotation | unknown; probably_damaging | ||
PolyPhen Variant Effect | unknown(ENST00000435723); probably_damaging(ENST00000393085) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.